Canonical Allele Identifier: CA1189448553
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112708178A= , CM000663.2:g.112708178A= GRCh38
NC_000001.10:g.113250800A= , CM000663.1:g.113250800A= GRCh37
NC_000001.9:g.113052323A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471038.6:n.428+2282T=
ENST00000605933.5:c.414+2282T=
ENST00000606505.5:c.414+2282T=
ENST00000606954.1:c.350+2282T=
ENST00000607158.5:n.477+2282T=