Canonical Allele Identifier: CA1168497150
Gene:

Linked Data

dbSNP Id: rs1644496998

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56262289T>A , CM000663.2:g.56262289T>A GRCh38
NC_000001.10:g.56727961T>A , CM000663.1:g.56727961T>A GRCh37
NC_000001.9:g.56500549T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.760-13089A>T ENSP00000493138.1:n.760-13089A>T
ENST00000641346.1:c.367-13089A>T
ENST00000641415.1:c.193-8396A>T
ENST00000641494.1:c.379-13089A>T
ENST00000642129.1:c.769-13089A>T