Canonical Allele Identifier: CA1259810655
Gene: ATP6V1B1 HGNC NCBI
VAX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70958106C= , CM000664.2:g.70958106C= GRCh38
NC_000002.11:g.71185236C= , CM000664.1:g.71185236C= GRCh37
NC_000002.10:g.71038744C= NCBI36
NG_008016.1:g.27239C=

Transcript Alleles

HGVS Amino-acid change
ENST00000234396.10:c.235C= (ATP6V1B1) MANE Select ENSP00000234396.4:p.Gln79=
ENST00000432098.2:n.401C= (ATP6V1B1)
ENST00000432367.6:c.439C= (VAX2)
ENST00000454446.6:c.235C= (ATP6V1B1) ENSP00000408361.2:p.Gln79=
ENST00000646783.1:c.271C= (VAX2)
ENST00000234396.8:c.235C= (ATP6V1B1) ENSP00000234396.4:p.Gln79=
ENST00000412314.5:c.235C= (ATP6V1B1) ENSP00000388353.1:p.Gln79=
ENST00000432098.1:c.-126C= (ATP6V1B1) ENSP00000387599.1:n.-126C=
ENST00000432367.5:c.235C= (ATP6V1B1) ENSP00000405114.1:p.Gln79=
ENST00000453130.1:c.143-9731G=
ENST00000454446.5:c.286C= (ATP6V1B1) ENSP00000408361.1:p.Gln96=
ENST00000463380.1:n.336C= (ATP6V1B1)
ENST00000606025.5:c.476-15673G= ENSP00000475641.1:n.476-15673G=
NM_001692.3:c.235C= (ATP6V1B1) NP_001683.2:p.Gln79=
XM_011532907.1:c.355C= (ATP6V1B1) XP_011531209.1:p.Gln119=
NM_001692.4:c.235C= (ATP6V1B1) MANE Select NP_001683.2:p.Gln79=
XM_011532907.2:c.355C= (ATP6V1B1) XP_011531209.1:p.Gln119=