Canonical Allele Identifier: CA1259810652

Gene: ATP6V1B1 VAX2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70958105G= , CM000664.2:g.70958105G=	GRCh38
NC_000002.11:g.71185235G= , CM000664.1:g.71185235G=	GRCh37
NC_000002.10:g.71038743G=	NCBI36
NG_008016.1:g.27238G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234396.10:c.234G= (ATP6V1B1) MANE Select	ENSP00000234396.4:p.Gly78=
ENST00000432098.2:n.400G= (ATP6V1B1)
ENST00000432367.6:c.438G= (VAX2)
ENST00000454446.6:c.234G= (ATP6V1B1)	ENSP00000408361.2:p.Gly78=
ENST00000646783.1:c.270G= (VAX2)
ENST00000234396.8:c.234G= (ATP6V1B1)	ENSP00000234396.4:p.Gly78=
ENST00000412314.5:c.234G= (ATP6V1B1)	ENSP00000388353.1:p.Gly78=
ENST00000432098.1:c.-127G= (ATP6V1B1)	ENSP00000387599.1:n.-127G=
ENST00000432367.5:c.234G= (ATP6V1B1)	ENSP00000405114.1:p.Gly78=
ENST00000453130.1:c.143-9730C=
ENST00000454446.5:c.285G= (ATP6V1B1)	ENSP00000408361.1:p.Gly95=
ENST00000463380.1:n.335G= (ATP6V1B1)
ENST00000606025.5:c.476-15672C=	ENSP00000475641.1:n.476-15672C=
NM_001692.3:c.234G= (ATP6V1B1)	NP_001683.2:p.Gly78=
XM_011532907.1:c.354G= (ATP6V1B1)	XP_011531209.1:p.Gly118=
NM_001692.4:c.234G= (ATP6V1B1) MANE Select	NP_001683.2:p.Gly78=
XM_011532907.2:c.354G= (ATP6V1B1)	XP_011531209.1:p.Gly118=