Canonical Allele Identifier: CA1259810562

Gene: ATP6V1B1 VAX2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70957907C= , CM000664.2:g.70957907C=	GRCh38
NC_000002.11:g.71185037C= , CM000664.1:g.71185037C=	GRCh37
NC_000002.10:g.71038545C=	NCBI36
NG_008016.1:g.27040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234396.10:c.175-139C= (ATP6V1B1) MANE Select	ENSP00000234396.4:n.175-139C=
ENST00000432098.2:n.341-139C= (ATP6V1B1)
ENST00000432367.6:c.379-139C= (VAX2)
ENST00000454446.6:c.175-139C= (ATP6V1B1)	ENSP00000408361.2:n.175-139C=
ENST00000646783.1:c.211-139C= (VAX2)
ENST00000234396.8:c.175-139C= (ATP6V1B1)	ENSP00000234396.4:n.175-139C=
ENST00000412314.5:c.175-139C= (ATP6V1B1)	ENSP00000388353.1:n.175-139C=
ENST00000432098.1:c.-186-139C= (ATP6V1B1)	ENSP00000387599.1:n.-186-139C=
ENST00000432367.5:c.175-139C= (ATP6V1B1)	ENSP00000405114.1:n.175-139C=
ENST00000453130.1:c.143-9532G=
ENST00000454446.5:c.226-139C= (ATP6V1B1)	ENSP00000408361.1:n.226-139C=
ENST00000463380.1:n.137C= (ATP6V1B1)
ENST00000606025.5:c.476-15474G=	ENSP00000475641.1:n.476-15474G=
NM_001692.3:c.175-139C= (ATP6V1B1)	NP_001683.2:n.175-139C=
XM_011532907.1:c.295-139C= (ATP6V1B1)	XP_011531209.1:n.295-139C=
NM_001692.4:c.175-139C= (ATP6V1B1) MANE Select	NP_001683.2:n.175-139C=
XM_011532907.2:c.295-139C= (ATP6V1B1)	XP_011531209.1:n.295-139C=