Canonical Allele Identifier: CA549812893
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578130C>T , CM000666.2:g.12578130C>T GRCh38
NC_000004.11:g.12579754C>T , CM000666.1:g.12579754C>T GRCh37
NC_000004.10:g.12188852C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31212G>A
XR_001741374.1:n.254+44525G>A
XR_925406.3:n.140+31212G>A