Canonical Allele Identifier: CA387153855

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124220089A>C (hg19) ; chr12:g.123735542A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123735542A>C , CM000674.2:g.123735542A>C	GRCh38
NC_000012.11:g.124220089A>C , CM000674.1:g.124220089A>C	GRCh37
NC_000012.10:g.122786042A>C	NCBI36
NG_012743.1:g.28225A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330342.8:c.743A>C MANE Select	ENSP00000332247.2:p.His248Pro
ENST00000540368.6:n.774A>C
ENST00000613625.5:c.743A>C	ENSP00000482236.1:p.His248Pro
ENST00000674794.1:c.183A>C
ENST00000675344.1:c.743A>C	ENSP00000501953.1:p.His248Pro
ENST00000330342.7:c.743A>C	ENSP00000332247.2:p.His248Pro
ENST00000504192.2:c.353A>C	ENSP00000443441.1:p.His118Pro
ENST00000540368.5:n.953A>C
ENST00000545059.5:n.3379A>C
ENST00000613625.4:c.743A>C	ENSP00000482236.1:p.His248Pro
NM_012463.3:c.743A>C	NP_036595.2:p.His248Pro
XM_005253563.1:c.743A>C	XP_005253620.1:p.His248Pro
XM_006719317.2:c.230A>C	XP_006719380.1:p.His77Pro
XR_429088.1:n.906A>C
XM_024448910.1:c.743A>C	XP_024304678.1:p.His248Pro
XM_024448911.1:c.230A>C	XP_024304679.1:p.His77Pro
NM_012463.4:c.743A>C MANE Select	NP_036595.2:p.His248Pro