Canonical Allele Identifier: CA13641214
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4381679A>C , CM000674.2:g.4381679A>C GRCh38
NC_000012.11:g.4490845A>C , CM000674.1:g.4490845A>C GRCh37
NC_000012.10:g.4361106A>C NCBI36
NG_007087.1:g.3050T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648100.1:c.*1967+15397A>C ENSP00000497536.1:n.*1967+15397A>C
ENST00000674624.1:c.*1204+15397A>C ENSP00000501898.1:n.*1204+15397A>C