Canonical Allele Identifier: CA2796998971
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293205C>T , CM000674.2:g.93293205C>T GRCh38
NC_000012.11:g.93686981C>T , CM000674.1:g.93686981C>T GRCh37
NC_000012.10:g.92211112C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34822G>A