Canonical Allele Identifier: CA1259810633

Gene: ATP6V1B1 VAX2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70958069C= , CM000664.2:g.70958069C=	GRCh38
NC_000002.11:g.71185199C= , CM000664.1:g.71185199C=	GRCh37
NC_000002.10:g.71038707C=	NCBI36
NG_008016.1:g.27202C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234396.10:c.198C= (ATP6V1B1) MANE Select	ENSP00000234396.4:p.Val66=
ENST00000432098.2:n.364C= (ATP6V1B1)
ENST00000432367.6:c.402C= (VAX2)
ENST00000454446.6:c.198C= (ATP6V1B1)	ENSP00000408361.2:p.Val66=
ENST00000646783.1:c.234C= (VAX2)
ENST00000234396.8:c.198C= (ATP6V1B1)	ENSP00000234396.4:p.Val66=
ENST00000412314.5:c.198C= (ATP6V1B1)	ENSP00000388353.1:p.Val66=
ENST00000432098.1:c.-163C= (ATP6V1B1)	ENSP00000387599.1:n.-163C=
ENST00000432367.5:c.198C= (ATP6V1B1)	ENSP00000405114.1:p.Val66=
ENST00000453130.1:c.143-9694G=
ENST00000454446.5:c.249C= (ATP6V1B1)	ENSP00000408361.1:p.Val83=
ENST00000463380.1:n.299C= (ATP6V1B1)
ENST00000606025.5:c.476-15636G=	ENSP00000475641.1:n.476-15636G=
NM_001692.3:c.198C= (ATP6V1B1)	NP_001683.2:p.Val66=
XM_011532907.1:c.318C= (ATP6V1B1)	XP_011531209.1:p.Val106=
NM_001692.4:c.198C= (ATP6V1B1) MANE Select	NP_001683.2:p.Val66=
XM_011532907.2:c.318C= (ATP6V1B1)	XP_011531209.1:p.Val106=