Canonical Allele Identifier: CA426692699

Gene: ATP6V1B1 VAX2

Linked Data

• MyVariant Identifiers: chr2:g.71185265G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70958135G>C , CM000664.2:g.70958135G>C	GRCh38
NC_000002.11:g.71185265G>C , CM000664.1:g.71185265G>C	GRCh37
NC_000002.10:g.71038773G>C	NCBI36
NG_008016.1:g.27268G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234396.10:c.264G>C (ATP6V1B1) MANE Select	ENSP00000234396.4:p.Ala88=
ENST00000432098.2:n.430G>C (ATP6V1B1)
ENST00000432367.6:c.468G>C (VAX2)
ENST00000454446.6:c.264G>C (ATP6V1B1)	ENSP00000408361.2:p.Ala88=
ENST00000646783.1:c.300G>C (VAX2)
ENST00000234396.8:c.264G>C (ATP6V1B1)	ENSP00000234396.4:p.Ala88=
ENST00000412314.5:c.264G>C (ATP6V1B1)	ENSP00000388353.1:p.Ala88=
ENST00000432098.1:c.-97G>C (ATP6V1B1)	ENSP00000387599.1:n.-97G>C
ENST00000432367.5:c.264G>C (ATP6V1B1)	ENSP00000405114.1:p.Ala88=
ENST00000453130.1:c.143-9760C>G
ENST00000454446.5:c.315G>C (ATP6V1B1)	ENSP00000408361.1:p.Ala105=
ENST00000463380.1:n.365G>C (ATP6V1B1)
ENST00000606025.5:c.476-15702C>G	ENSP00000475641.1:n.476-15702C>G
NM_001692.3:c.264G>C (ATP6V1B1)	NP_001683.2:p.Ala88=
XM_011532907.1:c.384G>C (ATP6V1B1)	XP_011531209.1:p.Ala128=
NM_001692.4:c.264G>C (ATP6V1B1) MANE Select	NP_001683.2:p.Ala88=
XM_011532907.2:c.384G>C (ATP6V1B1)	XP_011531209.1:p.Ala128=