Canonical Allele Identifier: CA1259813780
Gene: ATP6V1B1 HGNC NCBI
VAX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70964966G= , CM000664.2:g.70964966G= GRCh38
NC_000002.11:g.71192096G= , CM000664.1:g.71192096G= GRCh37
NC_000002.10:g.71045604G= NCBI36
NG_008016.1:g.34099G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234396.10:c.1387G= (ATP6V1B1) MANE Select ENSP00000234396.4:p.Glu463=
ENST00000432367.6:c.1440G= (VAX2)
ENST00000433895.2:c.319G= (ATP6V1B1) ENSP00000407840.2:p.Glu107=
ENST00000234396.8:c.1387G= (ATP6V1B1) ENSP00000234396.4:p.Glu463=
ENST00000412314.5:c.1336G= (ATP6V1B1) ENSP00000388353.1:p.Glu446=
ENST00000432367.5:c.*665G= (ATP6V1B1) ENSP00000405114.1:n.*665G=
ENST00000433895.1:c.202G= (ATP6V1B1) ENSP00000407840.1:p.Glu68=
ENST00000453130.1:c.143-16591C=
ENST00000606025.5:c.476-22533C= ENSP00000475641.1:n.476-22533C=
NM_001692.3:c.1387G= (ATP6V1B1) NP_001683.2:p.Glu463=
XM_011532907.1:c.1507G= (ATP6V1B1) XP_011531209.1:p.Glu503=
NM_001692.4:c.1387G= (ATP6V1B1) MANE Select NP_001683.2:p.Glu463=
XM_011532907.2:c.1507G= (ATP6V1B1) XP_011531209.1:p.Glu503=