Canonical Allele Identifier: CA436714885
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 1037483
ClinVar RCV Id: RCV001340643
dbSNP Id: rs1777958465
gnomAD v3: 3-169764679-T-C
gnomAD v4: 3-169764679-T-C
MyVariant Identifiers: chr3:g.169482467T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764679T>C , CM000665.2:g.169764679T>C GRCh38
NC_000003.11:g.169482467T>C , CM000665.1:g.169482467T>C GRCh37
NC_000003.10:g.170965161T>C NCBI36
NG_016363.1:g.5382A>G , LRG_347:g.5382A>G

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.382A>G , LRG_347t1:n.382A>G
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