Canonical Allele Identifier: CA87961476
Gene:

Linked Data

dbSNP Id: rs75316749

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169043635A>G , CM000665.2:g.169043635A>G GRCh38
NC_000003.11:g.168761423A>G , CM000665.1:g.168761423A>G GRCh37
NC_000003.10:g.170244117A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001740574.1:n.90-11827T>C