Canonical Allele Identifier: CA2773674431
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817652A>G , CM000668.2:g.155817652A>G GRCh38
NC_000006.11:g.156138786A>G , CM000668.1:g.156138786A>G GRCh37
NC_000006.10:g.156180478A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+24233A>G
XR_943146.1:n.552-2982T>C
XR_001744423.1:n.606-2982T>C
XR_001744424.1:n.79+24233A>G