Canonical Allele Identifier: CA347180547

Gene: ATP6V1B1 VAX2

Linked Data

• MyVariant Identifiers: chr2:g.71185198T>A (hg19) ; chr2:g.70958068T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70958068T>A , CM000664.2:g.70958068T>A	GRCh38
NC_000002.11:g.71185198T>A , CM000664.1:g.71185198T>A	GRCh37
NC_000002.10:g.71038706T>A	NCBI36
NG_008016.1:g.27201T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234396.10:c.197T>A (ATP6V1B1) MANE Select	ENSP00000234396.4:p.Val66Asp
ENST00000432098.2:n.363T>A (ATP6V1B1)
ENST00000432367.6:c.401T>A (VAX2)
ENST00000454446.6:c.197T>A (ATP6V1B1)	ENSP00000408361.2:p.Val66Asp
ENST00000646783.1:c.233T>A (VAX2)
ENST00000234396.8:c.197T>A (ATP6V1B1)	ENSP00000234396.4:p.Val66Asp
ENST00000412314.5:c.197T>A (ATP6V1B1)	ENSP00000388353.1:p.Val66Asp
ENST00000432098.1:c.-164T>A (ATP6V1B1)	ENSP00000387599.1:n.-164T>A
ENST00000432367.5:c.197T>A (ATP6V1B1)	ENSP00000405114.1:p.Val66Asp
ENST00000453130.1:c.143-9693A>T
ENST00000454446.5:c.248T>A (ATP6V1B1)	ENSP00000408361.1:p.Val83Asp
ENST00000463380.1:n.298T>A (ATP6V1B1)
ENST00000606025.5:c.476-15635A>T	ENSP00000475641.1:n.476-15635A>T
NM_001692.3:c.197T>A (ATP6V1B1)	NP_001683.2:p.Val66Asp
XM_011532907.1:c.317T>A (ATP6V1B1)	XP_011531209.1:p.Val106Asp
NM_001692.4:c.197T>A (ATP6V1B1) MANE Select	NP_001683.2:p.Val66Asp
XM_011532907.2:c.317T>A (ATP6V1B1)	XP_011531209.1:p.Val106Asp