Canonical Allele Identifier: CA1284674196
Gene:

Linked Data

dbSNP Id: rs1680374673

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884053T>A , CM000664.2:g.122884053T>A GRCh38
NC_000002.11:g.123641629T>A , CM000664.1:g.123641629T>A GRCh37
NC_000002.10:g.123358099T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-889T>A
XR_001739692.1:n.1451-889T>A
XR_923292.2:n.1358-889T>A