Canonical Allele Identifier: CA2055289498
Gene:

Linked Data

dbSNP Id: rs1873066729

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293128T>G , CM000674.2:g.93293128T>G GRCh38
NC_000012.11:g.93686904T>G , CM000674.1:g.93686904T>G GRCh37
NC_000012.10:g.92211035T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34899A>C