Canonical Allele Identifier: CA1365145671
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057109C= , CM000665.2:g.53057109C= GRCh38
NC_000003.11:g.53091125C= , CM000665.1:g.53091125C= GRCh37
NC_000003.10:g.53066165C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9870G=
ENST00000607283.5:c.465-13855G=
ENST00000607495.5:c.447+20579G=