Canonical Allele Identifier: CA2649624317
Gene:

Linked Data

dbSNP Id: rs765509088

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121833G>A , CM000663.2:g.193121833G>A GRCh38
NC_000001.10:g.193090963G>A , CM000663.1:g.193090963G>A GRCh37
NC_000001.9:g.191357586G>A NCBI36
NG_012691.1:g.4876G>A , LRG_507:g.4876G>A

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1824C>T