Allele Registry

Canonical Allele Identifier: CA148055708

Gene: TARID HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.133539207A>G

GRCh37 chr6:g.133860345A>G

Linked Data - Sequence & Population

gnomAD v2:

6:133860345 A / G

gnomAD v3:

6:133539207 A / G

gnomAD v4:

6:133539207 A / G

Linked Data - NCBI & NCI

dbSNP:

9402515

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133539207A>G , CM000668.2:g.133539207A>G	GRCh38
NC_000006.11:g.133860345A>G , CM000668.1:g.133860345A>G	GRCh37
NC_000006.10:g.133902038A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.707-1849T>C

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