Canonical Allele Identifier: CA1365145567
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056883A= , CM000665.2:g.53056883A= GRCh38
NC_000003.11:g.53090899A= , CM000665.1:g.53090899A= GRCh37
NC_000003.10:g.53065939A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9644T=
ENST00000607283.5:c.465-13629T=
ENST00000607495.5:c.447+20805T=