Canonical Allele Identifier: CA426692454

Gene: ATP6V1B1 VAX2

Linked Data

• MyVariant Identifiers: chr2:g.71185214A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70958084A>C , CM000664.2:g.70958084A>C	GRCh38
NC_000002.11:g.71185214A>C , CM000664.1:g.71185214A>C	GRCh37
NC_000002.10:g.71038722A>C	NCBI36
NG_008016.1:g.27217A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234396.10:c.213A>C (ATP6V1B1) MANE Select	ENSP00000234396.4:p.Pro71=
ENST00000432098.2:n.379A>C (ATP6V1B1)
ENST00000432367.6:c.417A>C (VAX2)
ENST00000454446.6:c.213A>C (ATP6V1B1)	ENSP00000408361.2:p.Pro71=
ENST00000646783.1:c.249A>C (VAX2)
ENST00000234396.8:c.213A>C (ATP6V1B1)	ENSP00000234396.4:p.Pro71=
ENST00000412314.5:c.213A>C (ATP6V1B1)	ENSP00000388353.1:p.Pro71=
ENST00000432098.1:c.-148A>C (ATP6V1B1)	ENSP00000387599.1:n.-148A>C
ENST00000432367.5:c.213A>C (ATP6V1B1)	ENSP00000405114.1:p.Pro71=
ENST00000453130.1:c.143-9709T>G
ENST00000454446.5:c.264A>C (ATP6V1B1)	ENSP00000408361.1:p.Pro88=
ENST00000463380.1:n.314A>C (ATP6V1B1)
ENST00000606025.5:c.476-15651T>G	ENSP00000475641.1:n.476-15651T>G
NM_001692.3:c.213A>C (ATP6V1B1)	NP_001683.2:p.Pro71=
XM_011532907.1:c.333A>C (ATP6V1B1)	XP_011531209.1:p.Pro111=
NM_001692.4:c.213A>C (ATP6V1B1) MANE Select	NP_001683.2:p.Pro71=
XM_011532907.2:c.333A>C (ATP6V1B1)	XP_011531209.1:p.Pro111=