Canonical Allele Identifier: CA2580957608
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100101678G>T , CM000672.2:g.100101678G>T GRCh38
NC_000010.10:g.101861435G>T , CM000672.1:g.101861435G>T GRCh37
NC_000010.9:g.101851425G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946245.1:n.185+5441G>T