Canonical Allele Identifier: CA347180603
Gene: ATP6V1B1 HGNC NCBI
VAX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70958079C>G , CM000664.2:g.70958079C>G GRCh38
NC_000002.11:g.71185209C>G , CM000664.1:g.71185209C>G GRCh37
NC_000002.10:g.71038717C>G NCBI36
NG_008016.1:g.27212C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234396.10:c.208C>G (ATP6V1B1) MANE Select ENSP00000234396.4:p.Leu70Val
ENST00000432098.2:n.374C>G (ATP6V1B1)
ENST00000432367.6:c.412C>G (VAX2)
ENST00000454446.6:c.208C>G (ATP6V1B1) ENSP00000408361.2:p.Leu70Val
ENST00000646783.1:c.244C>G (VAX2)
ENST00000234396.8:c.208C>G (ATP6V1B1) ENSP00000234396.4:p.Leu70Val
ENST00000412314.5:c.208C>G (ATP6V1B1) ENSP00000388353.1:p.Leu70Val
ENST00000432098.1:c.-153C>G (ATP6V1B1) ENSP00000387599.1:n.-153C>G
ENST00000432367.5:c.208C>G (ATP6V1B1) ENSP00000405114.1:p.Leu70Val
ENST00000453130.1:c.143-9704G>C
ENST00000454446.5:c.259C>G (ATP6V1B1) ENSP00000408361.1:p.Leu87Val
ENST00000463380.1:n.309C>G (ATP6V1B1)
ENST00000606025.5:c.476-15646G>C ENSP00000475641.1:n.476-15646G>C
NM_001692.3:c.208C>G (ATP6V1B1) NP_001683.2:p.Leu70Val
XM_011532907.1:c.328C>G (ATP6V1B1) XP_011531209.1:p.Leu110Val
NM_001692.4:c.208C>G (ATP6V1B1) MANE Select NP_001683.2:p.Leu70Val
XM_011532907.2:c.328C>G (ATP6V1B1) XP_011531209.1:p.Leu110Val