Canonical Allele Identifier: CA482270737
Gene: ATP6V0A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.124220081C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123735534C>T , CM000674.2:g.123735534C>T GRCh38
NC_000012.11:g.124220081C>T , CM000674.1:g.124220081C>T GRCh37
NC_000012.10:g.122786034C>T NCBI36
NG_012743.1:g.28217C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330342.8:c.735C>T MANE Select ENSP00000332247.2:p.Tyr245=
ENST00000540368.6:n.766C>T
ENST00000613625.5:c.735C>T ENSP00000482236.1:p.Tyr245=
ENST00000674794.1:c.175C>T
ENST00000675344.1:c.735C>T ENSP00000501953.1:p.Tyr245=
ENST00000330342.7:c.735C>T ENSP00000332247.2:p.Tyr245=
ENST00000504192.2:c.345C>T ENSP00000443441.1:p.Tyr115=
ENST00000540368.5:n.945C>T
ENST00000545059.5:n.3371C>T
ENST00000613625.4:c.735C>T ENSP00000482236.1:p.Tyr245=
NM_012463.3:c.735C>T NP_036595.2:p.Tyr245=
XM_005253563.1:c.735C>T XP_005253620.1:p.Tyr245=
XM_006719317.2:c.222C>T XP_006719380.1:p.Tyr74=
XR_429088.1:n.898C>T
XM_024448910.1:c.735C>T XP_024304678.1:p.Tyr245=
XM_024448911.1:c.222C>T XP_024304679.1:p.Tyr74=
NM_012463.4:c.735C>T MANE Select NP_036595.2:p.Tyr245=