Canonical Allele Identifier: CA2510353874
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385019T>A , CM000663.2:g.56385019T>A GRCh38
NC_000001.10:g.56850691T>A , CM000663.1:g.56850691T>A GRCh37
NC_000001.9:g.56623279T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.759+93867A>T ENSP00000493138.1:n.759+93867A>T
ENST00000641346.1:c.366+15075A>T
ENST00000641415.1:c.192+98244A>T
ENST00000641494.1:c.378+98244A>T
ENST00000642129.1:c.768+98244A>T