Canonical Allele Identifier: CA17029189
Gene: TTC34 HGNC NCBI

Linked Data

dbSNP Id: rs149310312
gnomAD v3: 1-2792650-A-T
gnomAD v4: 1-2792650-A-T
MyVariant Identifiers: chr1:g.2709215A>T (hg19) chr1:g.2792650A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792650A>T , CM000663.2:g.2792650A>T GRCh38
NC_000001.10:g.2709215A>T , CM000663.1:g.2709215A>T GRCh37
NC_000001.9:g.2699075A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2304T>A MANE Select ENSP00000383873.4:n.785-2304T>A
ENST00000401095.8:c.785-2304T>A ENSP00000383873.4:n.785-2304T>A
NM_001242672.2:c.785-2304T>A NP_001229601.2:n.785-2304T>A
NM_001242672.3:c.785-2304T>A MANE Select NP_001229601.2:n.785-2304T>A
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