Canonical Allele Identifier: CA1365145573
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056897C= , CM000665.2:g.53056897C= GRCh38
NC_000003.11:g.53090913C= , CM000665.1:g.53090913C= GRCh37
NC_000003.10:g.53065953C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9658G=
ENST00000607283.5:c.465-13643G=
ENST00000607495.5:c.447+20791G=