Canonical Allele Identifier: CA371489301

Gene: TMEM70

Linked Data

• dbSNP Id: rs1815647947
• MyVariant Identifiers: chr8:g.74888641G>C (hg19) ; chr8:g.73976406G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73976406G>C , CM000670.2:g.73976406G>C	GRCh38
NC_000008.10:g.74888641G>C , CM000670.1:g.74888641G>C	GRCh37
NC_000008.9:g.75051195G>C	NCBI36
NG_016618.1:g.5265G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312184.6:c.125G>C MANE Select	ENSP00000312599.5:p.Ser42Thr
ENST00000312184.5:c.125G>C	ENSP00000312599.5:p.Ser42Thr
ENST00000416961.6:c.125G>C	ENSP00000407695.2:p.Ser42Thr
ENST00000517439.1:c.125G>C	ENSP00000429467.1:p.Ser42Thr
ENST00000517614.1:n.188G>C
ENST00000520167.5:n.317+445G>C
ENST00000523794.1:n.676G>C
NM_001040613.2:c.125G>C	NP_001035703.1:p.Ser42Thr
NM_017866.5:c.125G>C	NP_060336.3:p.Ser42Thr
NR_033334.1:n.265G>C
NM_017866.6:c.125G>C MANE Select	NP_060336.3:p.Ser42Thr
NM_001040613.3:c.125G>C	NP_001035703.1:p.Ser42Thr
NR_033334.2:n.212G>C