Canonical Allele Identifier: CA1168547955
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385015G= , CM000663.2:g.56385015G= GRCh38
NC_000001.10:g.56850687G= , CM000663.1:g.56850687G= GRCh37
NC_000001.9:g.56623275G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641109.1:c.759+93871C= ENSP00000493138.1:n.759+93871C=
ENST00000641346.1:c.366+15079C=
ENST00000641415.1:c.192+98248C=
ENST00000641494.1:c.378+98248C=
ENST00000642129.1:c.768+98248C=