Canonical Allele Identifier: CA1481405448
Gene:

Linked Data

dbSNP Id: rs1283426104

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499635C>G , CM000666.2:g.102499635C>G GRCh38
NC_000004.11:g.103420792C>G , CM000666.1:g.103420792C>G GRCh37
NC_000004.10:g.103639824C>G NCBI36
NG_050628.1:g.3307C>G

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1614G>C XP_011530769.1:n.643+1614G>C
NR_136202.1:n.48+2804G>C