Canonical Allele Identifier: CA1168547968
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385052A= , CM000663.2:g.56385052A= GRCh38
NC_000001.10:g.56850724A= , CM000663.1:g.56850724A= GRCh37
NC_000001.9:g.56623312A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641109.1:c.759+93834T= ENSP00000493138.1:n.759+93834T=
ENST00000641346.1:c.366+15042T=
ENST00000641415.1:c.192+98211T=
ENST00000641494.1:c.378+98211T=
ENST00000642129.1:c.768+98211T=