Canonical Allele Identifier: CA436715990
Gene: TERC HGNC NCBI

Linked Data

dbSNP Id: rs1248582778
gnomAD v2: 3-169482813-G-C
gnomAD v4: 3-169765025-G-C
MyVariant Identifiers: chr3:g.169482813G>C (hg19) chr3:g.169765025G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765025G>C , CM000665.2:g.169765025G>C GRCh38
NC_000003.11:g.169482813G>C , CM000665.1:g.169482813G>C GRCh37
NC_000003.10:g.170965507G>C NCBI36
NG_016363.1:g.5036C>G , LRG_347:g.5036C>G

Transcript Alleles

HGVS Amino-acid Change
NR_001566.1:n.36C>G , LRG_347t1:n.36C>G
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