Canonical Allele Identifier: CA347180497
Gene: ATP6V1B1 HGNC NCBI
VAX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70958059C>A , CM000664.2:g.70958059C>A GRCh38
NC_000002.11:g.71185189C>A , CM000664.1:g.71185189C>A GRCh37
NC_000002.10:g.71038697C>A NCBI36
NG_008016.1:g.27192C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234396.10:c.188C>A (ATP6V1B1) MANE Select ENSP00000234396.4:p.Ala63Glu
ENST00000432098.2:n.354C>A (ATP6V1B1)
ENST00000432367.6:c.392C>A (VAX2)
ENST00000454446.6:c.188C>A (ATP6V1B1) ENSP00000408361.2:p.Ala63Glu
ENST00000646783.1:c.224C>A (VAX2)
ENST00000234396.8:c.188C>A (ATP6V1B1) ENSP00000234396.4:p.Ala63Glu
ENST00000412314.5:c.188C>A (ATP6V1B1) ENSP00000388353.1:p.Ala63Glu
ENST00000432098.1:c.-173C>A (ATP6V1B1) ENSP00000387599.1:n.-173C>A
ENST00000432367.5:c.188C>A (ATP6V1B1) ENSP00000405114.1:p.Ala63Glu
ENST00000453130.1:c.143-9684G>T
ENST00000454446.5:c.239C>A (ATP6V1B1) ENSP00000408361.1:p.Ala80Glu
ENST00000463380.1:n.289C>A (ATP6V1B1)
ENST00000606025.5:c.476-15626G>T ENSP00000475641.1:n.476-15626G>T
NM_001692.3:c.188C>A (ATP6V1B1) NP_001683.2:p.Ala63Glu
XM_011532907.1:c.308C>A (ATP6V1B1) XP_011531209.1:p.Ala103Glu
NM_001692.4:c.188C>A (ATP6V1B1) MANE Select NP_001683.2:p.Ala63Glu
XM_011532907.2:c.308C>A (ATP6V1B1) XP_011531209.1:p.Ala103Glu