Canonical Allele Identifier: CA899319054
Gene:

Linked Data

dbSNP Id: rs11712655

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.135506407T>A , CM000665.2:g.135506407T>A GRCh38
NC_000003.11:g.135225249T>A , CM000665.1:g.135225249T>A GRCh37
NC_000003.10:g.136707939T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924527.1:n.225+9743A>T
XR_924528.1:n.225+9743A>T
XR_001740926.1:n.229+9743A>T
XR_002959651.1:n.229+9743A>T
XR_924527.3:n.229+9743A>T
XR_924528.3:n.229+9743A>T