Canonical Allele Identifier: CA54579250
Gene:

Linked Data

dbSNP Id: rs146493365

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079601G>A , CM000664.2:g.118079601G>A GRCh38
NC_000002.11:g.118837177G>A , CM000664.1:g.118837177G>A GRCh37
NC_000002.10:g.118553647G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2069C>T XP_011510607.1:n.697-2069C>T
XR_001739662.2:n.138+8650C>T