Canonical Allele Identifier: CA1286885942
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431642C= , CM000664.2:g.127431642C= GRCh38
NC_000002.11:g.128189218C= , CM000664.1:g.128189218C= GRCh37
NC_000002.10:g.127905688C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+25G=
XR_001739705.1:n.3607-3378G=
XR_923313.2:n.4042+25G=