Canonical Allele Identifier: CA103120288
Gene:

Linked Data

dbSNP Id: rs965677503

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499894A>G , CM000666.2:g.102499894A>G GRCh38
NC_000004.11:g.103421051A>G , CM000666.1:g.103421051A>G GRCh37
NC_000004.10:g.103640083A>G NCBI36
NG_050628.1:g.3566A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1355T>C XP_011530769.1:n.643+1355T>C
NR_136202.1:n.48+2545T>C