Canonical Allele Identifier: CA2699130881
Gene:

Linked Data

dbSNP Id: rs1668662906

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722524C>A , CM000664.2:g.52722524C>A GRCh38
NC_000002.11:g.52949662C>A , CM000664.1:g.52949662C>A GRCh37
NC_000002.10:g.52803166C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.733G>T