Canonical Allele Identifier: CA15080343
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110676298C>T , CM000663.2:g.110676298C>T GRCh38
NC_000001.10:g.111218920C>T , CM000663.1:g.111218920C>T GRCh37
NC_000001.9:g.111020443C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738182.1:n.569-10076C>T
XR_001738183.1:n.567-10076C>T
XR_001738184.1:n.573-10076C>T
XR_001738185.1:n.568-10076C>T
XR_001738186.1:n.572-10076C>T
XR_001738187.1:n.570-10076C>T