Canonical Allele Identifier: CA16124067
Gene:

Linked Data

dbSNP Id: rs11883722

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203936122G>A , CM000664.2:g.203936122G>A GRCh38
NC_000002.11:g.204800845G>A , CM000664.1:g.204800845G>A GRCh37
NC_000002.10:g.204509090G>A NCBI36
NG_011586.1:g.4343G>A , LRG_65:g.4343G>A

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.446C>T
XR_001739861.1:n.460C>T
XR_427213.3:n.460C>T