Canonical Allele Identifier: CA87624049
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 465766
ClinVar RCV Id: RCV000532612
dbSNP Id: rs906136164

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764830G>A , CM000665.2:g.169764830G>A GRCh38
NC_000003.11:g.169482618G>A , CM000665.1:g.169482618G>A GRCh37
NC_000003.10:g.170965312G>A NCBI36
NG_016363.1:g.5231C>T , LRG_347:g.5231C>T

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.231C>T , LRG_347t1:n.231C>T