Canonical Allele Identifier: CA10483125

Gene: TBC1D8B MORC4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.106840074A>G , CM000685.2:g.106840074A>G	GRCh38
NC_000023.10:g.106083304A>G , CM000685.1:g.106083304A>G	GRCh37
NC_000023.9:g.105969960A>G	NCBI36
NG_021284.1:g.42386A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_017752.3:c.1380A>G (TBC1D8B) MANE Select	NP_060222.2:p.Ser460=
ENST00000357242.10:c.1380A>G (TBC1D8B) MANE Select	ENSP00000349781.5:p.Ser460=
NM_017752.2:c.1380A>G (TBC1D8B)	NP_060222.2:p.Ser460=
NM_198881.1:c.1380A>G (TBC1D8B)	NP_942582.1:p.Ser460=
NM_198881.2:c.1380A>G (TBC1D8B)	NP_942582.1:p.Ser460=
ENST00000276175.7:c.1362A>G (TBC1D8B)	ENSP00000276175.3:p.Ser454=
ENST00000310452.6:c.1380A>G (TBC1D8B)	ENSP00000310675.2:p.Ser460=
ENST00000357242.9:c.1380A>G (TBC1D8B)	ENSP00000349781.5:p.Ser460=
ENST00000604604.1:c.112-24288T>C (MORC4)
XM_006724669.1:c.1230A>G (TBC1D8B)	XP_006724732.1:p.Ser410=
XM_006724670.2:c.1086A>G (TBC1D8B)	XP_006724733.1:p.Ser362=
XM_006724670.4:c.1086A>G (TBC1D8B)	XP_006724733.1:p.Ser362=
XR_001755701.1:n.1545A>G (TBC1D8B)