Canonical Allele Identifier: CA347180700
Gene: ATP6V1B1 HGNC NCBI
VAX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70958102C>A , CM000664.2:g.70958102C>A GRCh38
NC_000002.11:g.71185232C>A , CM000664.1:g.71185232C>A GRCh37
NC_000002.10:g.71038740C>A NCBI36
NG_008016.1:g.27235C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234396.10:c.231C>A (ATP6V1B1) MANE Select ENSP00000234396.4:p.Ser77Arg
ENST00000432098.2:n.397C>A (ATP6V1B1)
ENST00000432367.6:c.435C>A (VAX2)
ENST00000454446.6:c.231C>A (ATP6V1B1) ENSP00000408361.2:p.Ser77Arg
ENST00000646783.1:c.267C>A (VAX2)
ENST00000234396.8:c.231C>A (ATP6V1B1) ENSP00000234396.4:p.Ser77Arg
ENST00000412314.5:c.231C>A (ATP6V1B1) ENSP00000388353.1:p.Ser77Arg
ENST00000432098.1:c.-130C>A (ATP6V1B1) ENSP00000387599.1:n.-130C>A
ENST00000432367.5:c.231C>A (ATP6V1B1) ENSP00000405114.1:p.Ser77Arg
ENST00000453130.1:c.143-9727G>T
ENST00000454446.5:c.282C>A (ATP6V1B1) ENSP00000408361.1:p.Ser94Arg
ENST00000463380.1:n.332C>A (ATP6V1B1)
ENST00000606025.5:c.476-15669G>T ENSP00000475641.1:n.476-15669G>T
NM_001692.3:c.231C>A (ATP6V1B1) NP_001683.2:p.Ser77Arg
XM_011532907.1:c.351C>A (ATP6V1B1) XP_011531209.1:p.Ser117Arg
NM_001692.4:c.231C>A (ATP6V1B1) MANE Select NP_001683.2:p.Ser77Arg
XM_011532907.2:c.351C>A (ATP6V1B1) XP_011531209.1:p.Ser117Arg