Canonical Allele Identifier: CA1305906812
Gene:

Linked Data

dbSNP Id: rs1691193275

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260595A>G , CM000664.2:g.168260595A>G GRCh38
NC_000002.11:g.169117105A>G , CM000664.1:g.169117105A>G GRCh37
NC_000002.10:g.168825351A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739763.1:n.912-4501A>G
XR_001739764.1:n.318-4501A>G
XR_001739765.1:n.436-4501A>G