Canonical Allele Identifier: CA1365145734
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057257G= , CM000665.2:g.53057257G= GRCh38
NC_000003.11:g.53091273G= , CM000665.1:g.53091273G= GRCh37
NC_000003.10:g.53066313G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-10018C=
ENST00000607283.5:c.465-14003C=
ENST00000607495.5:c.447+20431C=