Canonical Allele Identifier: CA1581765817
Gene:

Linked Data

dbSNP Id: rs1758559696

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386905C>T , CM000667.2:g.129386905C>T GRCh38
NC_000005.9:g.128722598C>T , CM000667.1:g.128722598C>T GRCh37
NC_000005.8:g.128750497C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427770.2:n.163-1543C>T
XR_948774.1:n.235-5746C>T
XR_001742463.1:n.4089-1543C>T
XR_001742464.1:n.2019-5746C>T
XR_001742465.1:n.401-1543C>T
XR_427770.3:n.337-1543C>T