Canonical Allele Identifier: CA1769264733

Gene: ATP6V1B2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20208440A= , CM000670.2:g.20208440A=	GRCh38
NC_000008.10:g.20065951A= , CM000670.1:g.20065951A=	GRCh37
NC_000008.9:g.20110231A=	NCBI36
NG_047013.1:g.16248A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000276390.7:c.193-993A= MANE Select	ENSP00000276390.2:n.193-993A=
ENST00000276390.6:c.193-993A=	ENSP00000276390.2:n.193-993A=
ENST00000519667.1:c.161-993A=
ENST00000520830.1:c.301-993A=
ENST00000523478.5:c.193-1001A=	ENSP00000430154.1:n.193-1001A=
ENST00000523482.5:n.197-993A=
NM_001693.3:c.193-993A=	NP_001684.2:n.193-993A=
XR_002956632.1:n.225-993A=
XR_002956633.1:n.225-993A=
NM_001693.4:c.193-993A= MANE Select	NP_001684.2:n.193-993A=