Canonical Allele Identifier: CA1168547965
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385037A= , CM000663.2:g.56385037A= GRCh38
NC_000001.10:g.56850709A= , CM000663.1:g.56850709A= GRCh37
NC_000001.9:g.56623297A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.759+93849T= ENSP00000493138.1:n.759+93849T=
ENST00000641346.1:c.366+15057T=
ENST00000641415.1:c.192+98226T=
ENST00000641494.1:c.378+98226T=
ENST00000642129.1:c.768+98226T=