Canonical Allele Identifier: CA39003135
Gene:

Linked Data

dbSNP Id: rs900491983

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887081A>G , CM000663.2:g.224887081A>G GRCh38
NC_000001.10:g.225074783A>G , CM000663.1:g.225074783A>G GRCh37
NC_000001.9:g.223141406A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2300T>C
XR_949207.2:n.63-2300T>C