Canonical Allele Identifier: CA2726851572
Gene:

Linked Data

dbSNP Id: rs2121328862

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293105C>T , CM000674.2:g.93293105C>T GRCh38
NC_000012.11:g.93686881C>T , CM000674.1:g.93686881C>T GRCh37
NC_000012.10:g.92211012C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34922G>A