Canonical Allele Identifier: CA535800181
Gene:

Linked Data

dbSNP Id: rs1212275232

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883972G>A , CM000664.2:g.122883972G>A GRCh38
NC_000002.11:g.123641548G>A , CM000664.1:g.123641548G>A GRCh37
NC_000002.10:g.123358018G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-970G>A
XR_001739692.1:n.1451-970G>A
XR_923292.2:n.1358-970G>A