Canonical Allele Identifier: CA1839056748
Gene:

Linked Data

dbSNP Id: rs1823379260

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756094G>A , CM000671.2:g.21756094G>A GRCh38
NC_000009.11:g.21756093G>A , CM000671.1:g.21756093G>A GRCh37
NC_000009.10:g.21746093G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11731C>T