Canonical Allele Identifier: CA17029182
Gene: TTC34 HGNC NCBI

Linked Data

dbSNP Id: rs567924694
gnomAD v3: 1-2792633-G-C
gnomAD v4: 1-2792633-G-C
MyVariant Identifiers: chr1:g.2709198G>C (hg19) chr1:g.2792633G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792633G>C , CM000663.2:g.2792633G>C GRCh38
NC_000001.10:g.2709198G>C , CM000663.1:g.2709198G>C GRCh37
NC_000001.9:g.2699058G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2287C>G MANE Select ENSP00000383873.4:n.785-2287C>G
ENST00000401095.8:c.785-2287C>G ENSP00000383873.4:n.785-2287C>G
NM_001242672.2:c.785-2287C>G NP_001229601.2:n.785-2287C>G
NM_001242672.3:c.785-2287C>G MANE Select NP_001229601.2:n.785-2287C>G
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