Canonical Allele Identifier: CA2055289525
Gene:

Linked Data

dbSNP Id: rs1873068180

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293220A>G , CM000674.2:g.93293220A>G GRCh38
NC_000012.11:g.93686996A>G , CM000674.1:g.93686996A>G GRCh37
NC_000012.10:g.92211127A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34807T>C