Canonical Allele Identifier: CA12335109
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129540247T>C , CM000668.2:g.129540247T>C GRCh38
NC_000006.11:g.129861392T>C , CM000668.1:g.129861392T>C GRCh37
NC_000006.10:g.129903085T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942984.1:n.726+200A>G
XR_942985.1:n.590+200A>G
XR_001743859.1:n.682+200A>G
XR_001743860.1:n.682+200A>G
XR_001743861.1:n.682+200A>G
XR_001743863.1:n.682+200A>G
XR_002956395.1:n.5839+200A>G