Canonical Allele Identifier: CA2801197853
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384967G>T , CM000676.2:g.36384967G>T GRCh38
NC_000014.8:g.36854172G>T , CM000676.1:g.36854172G>T GRCh37
NC_000014.7:g.35923923G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12192G>T XP_011535730.1:n.319-12192G>T
XR_943756.1:n.358+23871G>T