Canonical Allele Identifier: CA2580594025
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.169420286T= , CM000668.2:g.169420286T= GRCh38
NC_000006.11:g.169820381T= , CM000668.1:g.169820381T= GRCh37
NC_000006.10:g.169562306T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648086.1:c.*875A= ENSP00000497979.1:n.*875A=
ENST00000650382.1:n.2014A=