Canonical Allele Identifier: CA784578957
Gene:

Linked Data

dbSNP Id: rs1200341598

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499617T>C , CM000666.2:g.102499617T>C GRCh38
NC_000004.11:g.103420774T>C , CM000666.1:g.103420774T>C GRCh37
NC_000004.10:g.103639806T>C NCBI36
NG_050628.1:g.3289T>C

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1632A>G XP_011530769.1:n.643+1632A>G
NR_136202.1:n.48+2822A>G