Canonical Allele Identifier: CA1081440031
Gene:

Linked Data

dbSNP Id: rs1758560689

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386975A>G , CM000667.2:g.129386975A>G GRCh38
NC_000005.9:g.128722668A>G , CM000667.1:g.128722668A>G GRCh37
NC_000005.8:g.128750567A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427770.2:n.163-1473A>G
XR_948774.1:n.235-5676A>G
XR_001742463.1:n.4089-1473A>G
XR_001742464.1:n.2019-5676A>G
XR_001742465.1:n.401-1473A>G
XR_427770.3:n.337-1473A>G