Canonical Allele Identifier: CA103120290
Gene:

Linked Data

dbSNP Id: rs918976845

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499924T>C , CM000666.2:g.102499924T>C GRCh38
NC_000004.11:g.103421081T>C , CM000666.1:g.103421081T>C GRCh37
NC_000004.10:g.103640113T>C NCBI36
NG_050628.1:g.3596T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1325A>G XP_011530769.1:n.643+1325A>G
NR_136202.1:n.48+2515A>G