Canonical Allele Identifier: CA2541800485
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293267T>G , CM000674.2:g.93293267T>G GRCh38
NC_000012.11:g.93687043T>G , CM000674.1:g.93687043T>G GRCh37
NC_000012.10:g.92211174T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34760A>C