Canonical Allele Identifier: CA1038979714
Gene:

Linked Data

dbSNP Id: rs1691193635

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260634A>G , CM000664.2:g.168260634A>G GRCh38
NC_000002.11:g.169117144A>G , CM000664.1:g.169117144A>G GRCh37
NC_000002.10:g.168825390A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739763.1:n.912-4462A>G
XR_001739764.1:n.318-4462A>G
XR_001739765.1:n.436-4462A>G