Canonical Allele Identifier: CA436716005
Gene: TERC HGNC NCBI

Linked Data

dbSNP Id: rs1336050074
MyVariant Identifiers: chr3:g.169482820A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765032A>C , CM000665.2:g.169765032A>C GRCh38
NC_000003.11:g.169482820A>C , CM000665.1:g.169482820A>C GRCh37
NC_000003.10:g.170965514A>C NCBI36
NG_016363.1:g.5029T>G , LRG_347:g.5029T>G

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.29T>G , LRG_347t1:n.29T>G