Canonical Allele Identifier: CA1189448559
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112708183A= , CM000663.2:g.112708183A= GRCh38
NC_000001.10:g.113250805A= , CM000663.1:g.113250805A= GRCh37
NC_000001.9:g.113052328A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471038.6:n.428+2277T=
ENST00000605933.5:c.414+2277T=
ENST00000606505.5:c.414+2277T=
ENST00000606954.1:c.350+2277T=
ENST00000607158.5:n.477+2277T=