Canonical Allele Identifier: CA734642569
Gene: TTC34 HGNC NCBI

Linked Data

dbSNP Id: rs1466597062
gnomAD v3: 1-2792611-T-C
gnomAD v4: 1-2792611-T-C
MyVariant Identifiers: chr1:g.2709176T>C (hg19) chr1:g.2792611T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792611T>C , CM000663.2:g.2792611T>C GRCh38
NC_000001.10:g.2709176T>C , CM000663.1:g.2709176T>C GRCh37
NC_000001.9:g.2699036T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2265A>G MANE Select ENSP00000383873.4:n.785-2265A>G
ENST00000401095.8:c.785-2265A>G ENSP00000383873.4:n.785-2265A>G
NM_001242672.2:c.785-2265A>G NP_001229601.2:n.785-2265A>G
NM_001242672.3:c.785-2265A>G MANE Select NP_001229601.2:n.785-2265A>G
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