Canonical Allele Identifier: CA1168497141
Gene:

Linked Data

dbSNP Id: rs947007

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56262266A>C , CM000663.2:g.56262266A>C GRCh38
NC_000001.10:g.56727938A>C , CM000663.1:g.56727938A>C GRCh37
NC_000001.9:g.56500526A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.760-13066T>G ENSP00000493138.1:n.760-13066T>G
ENST00000641346.1:c.367-13066T>G
ENST00000641415.1:c.193-8373T>G
ENST00000641494.1:c.379-13066T>G
ENST00000642129.1:c.769-13066T>G