Canonical Allele Identifier: CA343773620
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878762A>C (hg19) chr1:g.173909624A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909624A>C , CM000663.2:g.173909624A>C GRCh38
NC_000001.10:g.173878762A>C , CM000663.1:g.173878762A>C GRCh37
NC_000001.9:g.172145385A>C NCBI36
NG_012462.1:g.12755T>G , LRG_577:g.12755T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1081T>G MANE Select ENSP00000356671.3:p.Phe361Val
ENST00000367698.3:c.1081T>G ENSP00000356671.3:p.Phe361Val
ENST00000617423.4:c.560-2131T>G ENSP00000478688.1:n.560-2131T>G
NM_000488.3:c.1081T>G , LRG_577t1:c.1081T>G NP_000479.1:p.Phe361Val
XM_005245198.2:c.937T>G XP_005245255.1:p.Phe313Val
NM_001365052.1:c.937T>G NP_001351981.1:p.Phe313Val
NM_000488.4:c.1081T>G MANE Select NP_000479.1:p.Phe361Val
NM_001365052.2:c.937T>G NP_001351981.1:p.Phe313Val
NM_001386302.1:c.1204T>G NP_001373231.1:p.Phe402Val
NM_001386303.1:c.1162T>G NP_001373232.1:p.Phe388Val
NM_001386304.1:c.1060T>G NP_001373233.1:p.Phe354Val
NM_001386305.1:c.1024T>G NP_001373234.1:p.Phe342Val
NM_001386306.1:c.865T>G NP_001373235.1:p.Phe289Val
Search 100 bp 5'
Search 100 bp 3'