Canonical Allele Identifier: CA734642590
Gene: TTC34 HGNC NCBI

Linked Data

dbSNP Id: rs1377800791
MyVariant Identifiers: chr1:g.2709202G>A (hg19) chr1:g.2792637G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792637G>A , CM000663.2:g.2792637G>A GRCh38
NC_000001.10:g.2709202G>A , CM000663.1:g.2709202G>A GRCh37
NC_000001.9:g.2699062G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2291C>T MANE Select ENSP00000383873.4:n.785-2291C>T
ENST00000401095.8:c.785-2291C>T ENSP00000383873.4:n.785-2291C>T
NM_001242672.2:c.785-2291C>T NP_001229601.2:n.785-2291C>T
NM_001242672.3:c.785-2291C>T MANE Select NP_001229601.2:n.785-2291C>T
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