Canonical Allele Identifier: CA2695377689

Gene: TTC34

Linked Data

• dbSNP Id: rs2100632883

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2792709A>G , CM000663.2:g.2792709A>G	GRCh38
NC_000001.10:g.2709274A>G , CM000663.1:g.2709274A>G	GRCh37
NC_000001.9:g.2699134A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401095.9:c.785-2363T>C MANE Select	ENSP00000383873.4:n.785-2363T>C
ENST00000401095.8:c.785-2363T>C	ENSP00000383873.4:n.785-2363T>C
NM_001242672.2:c.785-2363T>C	NP_001229601.2:n.785-2363T>C
NM_001242672.3:c.785-2363T>C MANE Select	NP_001229601.2:n.785-2363T>C