Canonical Allele Identifier: CA54965482
Gene:

Linked Data

dbSNP Id: rs934980783

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368958G>A , CM000664.2:g.122368958G>A GRCh38
NC_000002.11:g.123126534G>A , CM000664.1:g.123126534G>A GRCh37
NC_000002.10:g.122843004G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24005G>A
XR_001739684.1:n.556-24005G>A