Canonical Allele Identifier: CA15463157
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155913388A>G , CM000668.2:g.155913388A>G GRCh38
NC_000006.11:g.156234522A>G , CM000668.1:g.156234522A>G GRCh37
NC_000006.10:g.156276214A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.669-1423A>G
XR_943143.1:n.1169-1423A>G
XR_943144.1:n.530-1423A>G
XR_943146.1:n.352-80494T>C
XR_001744423.1:n.406-80494T>C