Canonical Allele Identifier: CA1081439996
Gene:

Linked Data

dbSNP Id: rs1758558862

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386835C>G , CM000667.2:g.129386835C>G GRCh38
NC_000005.9:g.128722528C>G , CM000667.1:g.128722528C>G GRCh37
NC_000005.8:g.128750427C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427770.2:n.163-1613C>G
XR_948774.1:n.235-5816C>G
XR_001742463.1:n.4089-1613C>G
XR_001742464.1:n.2019-5816C>G
XR_001742465.1:n.401-1613C>G
XR_427770.3:n.337-1613C>G