Canonical Allele Identifier: CA891313715
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1300225544
gnomAD v4: 1-173910064-T-C
MyVariant Identifiers: chr1:g.173879202T>C (hg19) chr1:g.173910064T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910064T>C , CM000663.2:g.173910064T>C GRCh38
NC_000001.10:g.173879202T>C , CM000663.1:g.173879202T>C GRCh37
NC_000001.9:g.172145825T>C NCBI36
NG_012462.1:g.12315A>G , LRG_577:g.12315A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-122A>G MANE Select ENSP00000356671.3:n.763-122A>G
ENST00000367698.3:c.763-122A>G ENSP00000356671.3:n.763-122A>G
ENST00000487183.1:n.414-122A>G
ENST00000617423.4:c.559+1800A>G ENSP00000478688.1:n.559+1800A>G
NM_000488.3:c.763-122A>G , LRG_577t1:c.763-122A>G NP_000479.1:n.763-122A>G
XM_005245198.2:c.619-122A>G XP_005245255.1:n.619-122A>G
NM_001365052.1:c.619-122A>G NP_001351981.1:n.619-122A>G
NM_000488.4:c.763-122A>G MANE Select NP_000479.1:n.763-122A>G
NM_001365052.2:c.619-122A>G NP_001351981.1:n.619-122A>G
NM_001386302.1:c.886-122A>G NP_001373231.1:n.886-122A>G
NM_001386303.1:c.844-122A>G NP_001373232.1:n.844-122A>G
NM_001386304.1:c.742-122A>G NP_001373233.1:n.742-122A>G
NM_001386305.1:c.763-179A>G NP_001373234.1:n.763-179A>G
NM_001386306.1:c.547-122A>G NP_001373235.1:n.547-122A>G
Search 100 bp 5'
Search 100 bp 3'