Canonical Allele Identifier: CA54965479
Gene:

Linked Data

dbSNP Id: rs115614898

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368927G>A , CM000664.2:g.122368927G>A GRCh38
NC_000002.11:g.123126503G>A , CM000664.1:g.123126503G>A GRCh37
NC_000002.10:g.122842973G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24036G>A
XR_001739684.1:n.556-24036G>A