Canonical Allele Identifier: CA153770473
Gene:

Linked Data

dbSNP Id: rs981812074

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9816785A>G , CM000669.2:g.9816785A>G GRCh38
NC_000007.13:g.9856414A>G , CM000669.1:g.9856414A>G GRCh37
NC_000007.12:g.9822939A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927024.1:n.209+50005T>C
XR_927025.1:n.323+50005T>C
XR_927026.1:n.209+50005T>C
XR_927026.2:n.209+50005T>C