Canonical Allele Identifier: CA2796998969
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293075G>T , CM000674.2:g.93293075G>T GRCh38
NC_000012.11:g.93686851G>T , CM000674.1:g.93686851G>T GRCh37
NC_000012.10:g.92210982G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34952C>A