Canonical Allele Identifier: CA1250829248
Gene:

Linked Data

dbSNP Id: rs1668651900

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722195G>A , CM000664.2:g.52722195G>A GRCh38
NC_000002.11:g.52949333G>A , CM000664.1:g.52949333G>A GRCh37
NC_000002.10:g.52802837G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959384.1:n.1062C>T