Canonical Allele Identifier: CA2246165572
Gene:

Linked Data

dbSNP Id: rs1981887297

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137263G>T , CM000679.2:g.8137263G>T GRCh38
NC_000017.10:g.8040581G>T , CM000679.1:g.8040581G>T GRCh37
NC_000017.9:g.7981306G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1586G>T
XR_934203.1:n.70-2214G>T
XR_934202.2:n.414-1586G>T