Canonical Allele Identifier: CA950572598
Gene:

Linked Data

dbSNP Id: rs1873066111

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293104A>G , CM000674.2:g.93293104A>G GRCh38
NC_000012.11:g.93686880A>G , CM000674.1:g.93686880A>G GRCh37
NC_000012.10:g.92211011A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34923T>C