Canonical Allele Identifier: CA103120284
Gene:

Linked Data

dbSNP Id: rs954148704

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499866T>C , CM000666.2:g.102499866T>C GRCh38
NC_000004.11:g.103421023T>C , CM000666.1:g.103421023T>C GRCh37
NC_000004.10:g.103640055T>C NCBI36
NG_050628.1:g.3538T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1383A>G XP_011530769.1:n.643+1383A>G
NR_136202.1:n.48+2573A>G