Canonical Allele Identifier: CA347180443
Gene: ATP6V1B1 HGNC NCBI
VAX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70958048T>A , CM000664.2:g.70958048T>A GRCh38
NC_000002.11:g.71185178T>A , CM000664.1:g.71185178T>A GRCh37
NC_000002.10:g.71038686T>A NCBI36
NG_008016.1:g.27181T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234396.10:c.177T>A (ATP6V1B1) MANE Select ENSP00000234396.4:p.Phe59Leu
ENST00000432098.2:n.343T>A (ATP6V1B1)
ENST00000432367.6:c.381T>A (VAX2)
ENST00000454446.6:c.177T>A (ATP6V1B1) ENSP00000408361.2:p.Phe59Leu
ENST00000646783.1:c.213T>A (VAX2)
ENST00000234396.8:c.177T>A (ATP6V1B1) ENSP00000234396.4:p.Phe59Leu
ENST00000412314.5:c.177T>A (ATP6V1B1) ENSP00000388353.1:p.Phe59Leu
ENST00000432098.1:c.-184T>A (ATP6V1B1) ENSP00000387599.1:n.-184T>A
ENST00000432367.5:c.177T>A (ATP6V1B1) ENSP00000405114.1:p.Phe59Leu
ENST00000453130.1:c.143-9673A>T
ENST00000454446.5:c.228T>A (ATP6V1B1) ENSP00000408361.1:p.Phe76Leu
ENST00000463380.1:n.278T>A (ATP6V1B1)
ENST00000606025.5:c.476-15615A>T ENSP00000475641.1:n.476-15615A>T
NM_001692.3:c.177T>A (ATP6V1B1) NP_001683.2:p.Phe59Leu
XM_011532907.1:c.297T>A (ATP6V1B1) XP_011531209.1:p.Phe99Leu
NM_001692.4:c.177T>A (ATP6V1B1) MANE Select NP_001683.2:p.Phe59Leu
XM_011532907.2:c.297T>A (ATP6V1B1) XP_011531209.1:p.Phe99Leu