Canonical Allele Identifier: CA436714813
Gene: TERC HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764653G>A , CM000665.2:g.169764653G>A GRCh38
NC_000003.11:g.169482441G>A , CM000665.1:g.169482441G>A GRCh37
NC_000003.10:g.170965135G>A NCBI36
NG_016363.1:g.5408C>T , LRG_347:g.5408C>T

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.408C>T , LRG_347t1:n.408C>T