Canonical Allele Identifier: CA2055289494
Gene:

Linked Data

dbSNP Id: rs1873066536

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293114A>T , CM000674.2:g.93293114A>T GRCh38
NC_000012.11:g.93686890A>T , CM000674.1:g.93686890A>T GRCh37
NC_000012.10:g.92211021A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34913T>A