Canonical Allele Identifier: CA343756
Gene: TERC HGNC NCBI
ClinVar RCV:
RCV000032563
ClinVar Variation:
39284
dbSNP:
199422276
MyVariant.info:
GRCh38 chr3:g.169764881G>A
GRCh37 chr3:g.169482669G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764881G>A , CM000665.2:g.169764881G>A GRCh38
NC_000003.11:g.169482669G>A , CM000665.1:g.169482669G>A GRCh37
NC_000003.10:g.170965363G>A NCBI36
NG_016363.1:g.5180C>T , LRG_347:g.5180C>T

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.180C>T , LRG_347t1:n.180C>T
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