Canonical Allele Identifier: CA6861849

Gene: ATP6V0A2

Linked Data

• ClinVar Variation Id: 945705
• ClinVar RCV Id: RCV001760196 ; RCV001216411
• dbSNP Id: rs771839087
• ExAC: 12:124228411 A / G
• gnomAD v2: 12-124228411-A-G
• gnomAD v3: 12-123743864-A-G
• gnomAD v4: 12-123743864-A-G
• MyVariant Identifiers: chr12:g.124228411A>G (hg19) ; chr12:g.123743864A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123743864A>G , CM000674.2:g.123743864A>G	GRCh38
NC_000012.11:g.124228411A>G , CM000674.1:g.124228411A>G	GRCh37
NC_000012.10:g.122794364A>G	NCBI36
NG_012743.1:g.36547A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1118A>G MANE Select	ENSP00000332247.2:p.Asn373Ser
ENST00000540368.6:n.1149A>G
ENST00000674794.1:c.1206A>G
ENST00000675260.1:n.393A>G
ENST00000675344.1:c.*139A>G	ENSP00000501953.1:n.*139A>G
ENST00000330342.7:c.1118A>G	ENSP00000332247.2:p.Asn373Ser
ENST00000504192.2:c.728A>G	ENSP00000443441.1:p.Asn243Ser
ENST00000536426.1:n.135A>G
ENST00000545059.5:n.3754A>G
NM_012463.3:c.1118A>G	NP_036595.2:p.Asn373Ser
XM_005253563.1:c.1118A>G	XP_005253620.1:p.Asn373Ser
XM_006719317.2:c.605A>G	XP_006719380.1:p.Asn202Ser
XM_006719318.2:c.296A>G	XP_006719381.1:p.Asn99Ser
XR_429088.1:n.1281A>G
XM_024448910.1:c.1118A>G	XP_024304678.1:p.Asn373Ser
XM_024448911.1:c.605A>G	XP_024304679.1:p.Asn202Ser
XM_024448912.1:c.296A>G	XP_024304680.1:p.Asn99Ser
NM_012463.4:c.1118A>G MANE Select	NP_036595.2:p.Asn373Ser