Canonical Allele Identifier: CA347180841
Gene: ATP6V1B1 HGNC NCBI
VAX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70958137T>G , CM000664.2:g.70958137T>G GRCh38
NC_000002.11:g.71185267T>G , CM000664.1:g.71185267T>G GRCh37
NC_000002.10:g.71038775T>G NCBI36
NG_008016.1:g.27270T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234396.10:c.266T>G (ATP6V1B1) MANE Select ENSP00000234396.4:p.Ile89Ser
ENST00000432098.2:n.432T>G (ATP6V1B1)
ENST00000432367.6:c.470T>G (VAX2)
ENST00000454446.6:c.266T>G (ATP6V1B1) ENSP00000408361.2:p.Ile89Ser
ENST00000646783.1:c.302T>G (VAX2)
ENST00000234396.8:c.266T>G (ATP6V1B1) ENSP00000234396.4:p.Ile89Ser
ENST00000412314.5:c.266T>G (ATP6V1B1) ENSP00000388353.1:p.Ile89Ser
ENST00000432098.1:c.-95T>G (ATP6V1B1) ENSP00000387599.1:n.-95T>G
ENST00000432367.5:c.266T>G (ATP6V1B1) ENSP00000405114.1:p.Ile89Ser
ENST00000453130.1:c.143-9762A>C
ENST00000454446.5:c.317T>G (ATP6V1B1) ENSP00000408361.1:p.Ile106Ser
ENST00000463380.1:n.367T>G (ATP6V1B1)
ENST00000606025.5:c.476-15704A>C ENSP00000475641.1:n.476-15704A>C
NM_001692.3:c.266T>G (ATP6V1B1) NP_001683.2:p.Ile89Ser
XM_011532907.1:c.386T>G (ATP6V1B1) XP_011531209.1:p.Ile129Ser
NM_001692.4:c.266T>G (ATP6V1B1) MANE Select NP_001683.2:p.Ile89Ser
XM_011532907.2:c.386T>G (ATP6V1B1) XP_011531209.1:p.Ile129Ser