Canonical Allele Identifier: CA436715606
Gene: TERC HGNC NCBI

Linked Data

dbSNP Id: rs1466076069
gnomAD v2: 3-169482694-A-T
gnomAD v4: 3-169764906-A-T
MyVariant Identifiers: chr3:g.169482694A>T (hg19) chr3:g.169764906A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169764906A>T , CM000665.2:g.169764906A>T GRCh38
NC_000003.11:g.169482694A>T , CM000665.1:g.169482694A>T GRCh37
NC_000003.10:g.170965388A>T NCBI36
NG_016363.1:g.5155T>A , LRG_347:g.5155T>A

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.155T>A , LRG_347t1:n.155T>A
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Search 100 bp 3'