Canonical Allele Identifier: CA32780496
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1045759562
gnomAD v2: 1-173879144-A-C
gnomAD v3: 1-173910006-A-C
gnomAD v4: 1-173910006-A-C
MyVariant Identifiers: chr1:g.173879144A>C (hg19) chr1:g.173910006A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910006A>C , CM000663.2:g.173910006A>C GRCh38
NC_000001.10:g.173879144A>C , CM000663.1:g.173879144A>C GRCh37
NC_000001.9:g.172145767A>C NCBI36
NG_012462.1:g.12373T>G , LRG_577:g.12373T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-64T>G MANE Select ENSP00000356671.3:n.763-64T>G
ENST00000367698.3:c.763-64T>G ENSP00000356671.3:n.763-64T>G
ENST00000487183.1:n.414-64T>G
ENST00000617423.4:c.559+1858T>G ENSP00000478688.1:n.559+1858T>G
NM_000488.3:c.763-64T>G , LRG_577t1:c.763-64T>G NP_000479.1:n.763-64T>G
XM_005245198.2:c.619-64T>G XP_005245255.1:n.619-64T>G
NM_001365052.1:c.619-64T>G NP_001351981.1:n.619-64T>G
NM_000488.4:c.763-64T>G MANE Select NP_000479.1:n.763-64T>G
NM_001365052.2:c.619-64T>G NP_001351981.1:n.619-64T>G
NM_001386302.1:c.886-64T>G NP_001373231.1:n.886-64T>G
NM_001386303.1:c.844-64T>G NP_001373232.1:n.844-64T>G
NM_001386304.1:c.742-64T>G NP_001373233.1:n.742-64T>G
NM_001386305.1:c.763-121T>G NP_001373234.1:n.763-121T>G
NM_001386306.1:c.547-64T>G NP_001373235.1:n.547-64T>G
Search 100 bp 5'
Search 100 bp 3'