Canonical Allele Identifier: CA1305906748
Gene:

Linked Data

dbSNP Id: rs1042487558

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260456C>G , CM000664.2:g.168260456C>G GRCh38
NC_000002.11:g.169116966C>G , CM000664.1:g.169116966C>G GRCh37
NC_000002.10:g.168825212C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739763.1:n.912-4640C>G
XR_001739764.1:n.318-4640C>G
XR_001739765.1:n.436-4640C>G