Canonical Allele Identifier: CA2246165528
Gene:

Linked Data

dbSNP Id: rs932690439

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137231T>G , CM000679.2:g.8137231T>G GRCh38
NC_000017.10:g.8040549T>G , CM000679.1:g.8040549T>G GRCh37
NC_000017.9:g.7981274T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1618T>G
XR_934203.1:n.70-2246T>G
XR_934202.2:n.414-1618T>G