Canonical Allele Identifier: CA562920062
Gene:

Linked Data

dbSNP Id: rs1409475824

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386947G>A , CM000667.2:g.129386947G>A GRCh38
NC_000005.9:g.128722640G>A , CM000667.1:g.128722640G>A GRCh37
NC_000005.8:g.128750539G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427770.2:n.163-1501G>A
XR_948774.1:n.235-5704G>A
XR_001742463.1:n.4089-1501G>A
XR_001742464.1:n.2019-5704G>A
XR_001742465.1:n.401-1501G>A
XR_427770.3:n.337-1501G>A