Canonical Allele Identifier: CA1895268793
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.20610679T>A , CM000672.2:g.20610679T>A GRCh38
NC_000010.10:g.20899608T>A , CM000672.1:g.20899608T>A GRCh37
NC_000010.9:g.20939614T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930728.1:n.1231T>A
XR_930729.1:n.1276T>A
XR_930730.1:n.1127T>A
XR_930731.1:n.1060T>A
XR_930732.1:n.1082T>A
XR_930733.1:n.1131T>A
XR_001747381.1:n.6079T>A
XR_001747382.1:n.3160T>A
XR_001747383.1:n.5422T>A
XR_001747384.2:n.5273T>A
XR_930729.2:n.2503T>A
XR_930733.2:n.5377T>A