Canonical Allele Identifier: CA1081440033
Gene:

Linked Data

dbSNP Id: rs1205814004

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386983A>T , CM000667.2:g.129386983A>T GRCh38
NC_000005.9:g.128722676A>T , CM000667.1:g.128722676A>T GRCh37
NC_000005.8:g.128750575A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427770.2:n.163-1465A>T
XR_948774.1:n.235-5668A>T
XR_001742463.1:n.4089-1465A>T
XR_001742464.1:n.2019-5668A>T
XR_001742465.1:n.401-1465A>T
XR_427770.3:n.337-1465A>T