Canonical Allele Identifier: CA440619259
Gene:

Linked Data

dbSNP Id: rs1738958433
MyVariant Identifiers: chr4:g.103422137T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500980T>C , CM000666.2:g.102500980T>C GRCh38
NC_000004.11:g.103422137T>C , CM000666.1:g.103422137T>C GRCh37
NC_000004.10:g.103641169T>C NCBI36
NG_050628.1:g.4652T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+269A>G XP_011530769.1:n.643+269A>G
NR_136202.1:n.48+1459A>G