Canonical Allele Identifier: CA10483123

Gene: TBC1D8B MORC4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.106840015A>G , CM000685.2:g.106840015A>G	GRCh38
NC_000023.10:g.106083245A>G , CM000685.1:g.106083245A>G	GRCh37
NC_000023.9:g.105969901A>G	NCBI36
NG_021284.1:g.42327A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357242.10:c.1354-33A>G (TBC1D8B) MANE Select	ENSP00000349781.5:n.1354-33A>G
ENST00000276175.7:c.1336-33A>G (TBC1D8B)	ENSP00000276175.3:n.1336-33A>G
ENST00000310452.6:c.1354-33A>G (TBC1D8B)	ENSP00000310675.2:n.1354-33A>G
ENST00000357242.9:c.1354-33A>G (TBC1D8B)	ENSP00000349781.5:n.1354-33A>G
ENST00000604604.1:c.112-24229T>C (MORC4)
NM_017752.2:c.1354-33A>G (TBC1D8B)	NP_060222.2:n.1354-33A>G
NM_198881.1:c.1354-33A>G (TBC1D8B)	NP_942582.1:n.1354-33A>G
XM_006724669.1:c.1204-33A>G (TBC1D8B)	XP_006724732.1:n.1204-33A>G
XM_006724670.2:c.1060-33A>G (TBC1D8B)	XP_006724733.1:n.1060-33A>G
XM_006724670.4:c.1060-33A>G (TBC1D8B)	XP_006724733.1:n.1060-33A>G
XR_001755701.1:n.1519-33A>G (TBC1D8B)
NM_017752.3:c.1354-33A>G (TBC1D8B) MANE Select	NP_060222.2:n.1354-33A>G
NM_198881.2:c.1354-33A>G (TBC1D8B)	NP_942582.1:n.1354-33A>G