Canonical Allele Identifier: CA1318169422
Gene:

Linked Data

dbSNP Id: rs1688119207

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195006978G>A , CM000664.2:g.195006978G>A GRCh38
NC_000002.11:g.195871702G>A , CM000664.1:g.195871702G>A GRCh37
NC_000002.10:g.195579947G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739836.1:n.553+52457C>T