Canonical Allele Identifier: CA734642578

Gene: TTC34

Linked Data

• dbSNP Id: rs1246839236
• MyVariant Identifiers: chr1:g.2709186G>A (hg19) ; chr1:g.2792621G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2792621G>A , CM000663.2:g.2792621G>A	GRCh38
NC_000001.10:g.2709186G>A , CM000663.1:g.2709186G>A	GRCh37
NC_000001.9:g.2699046G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401095.9:c.785-2275C>T MANE Select	ENSP00000383873.4:n.785-2275C>T
ENST00000401095.8:c.785-2275C>T	ENSP00000383873.4:n.785-2275C>T
NM_001242672.2:c.785-2275C>T	NP_001229601.2:n.785-2275C>T
NM_001242672.3:c.785-2275C>T MANE Select	NP_001229601.2:n.785-2275C>T