Canonical Allele Identifier: CA997830988
Gene: TTC34 HGNC NCBI

Linked Data

dbSNP Id: rs1643675744
gnomAD v3: 1-2792678-T-G
gnomAD v4: 1-2792678-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792678T>G , CM000663.2:g.2792678T>G GRCh38
NC_000001.10:g.2709243T>G , CM000663.1:g.2709243T>G GRCh37
NC_000001.9:g.2699103T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2332A>C MANE Select ENSP00000383873.4:n.785-2332A>C
ENST00000401095.8:c.785-2332A>C ENSP00000383873.4:n.785-2332A>C
NM_001242672.2:c.785-2332A>C NP_001229601.2:n.785-2332A>C
NM_001242672.3:c.785-2332A>C MANE Select NP_001229601.2:n.785-2332A>C
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