Canonical Allele Identifier: CA607602471

Gene: ATP2A2

Linked Data

• dbSNP Id: rs1240742970
• gnomAD v2: 12-110783022-G-C
• gnomAD v4: 12-110345217-G-C
• MyVariant Identifiers: chr12:g.110783022G>C (hg19) ; chr12:g.110345217G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345217G>C , CM000674.2:g.110345217G>C	GRCh38
NC_000012.11:g.110783022G>C , CM000674.1:g.110783022G>C	GRCh37
NC_000012.10:g.109267405G>C	NCBI36
NG_007097.2:g.68591G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2608-32G>C MANE Select	ENSP00000440045.2:n.2608-32G>C
ENST00000308664.10:c.2608-32G>C	ENSP00000311186.6:n.2608-32G>C
ENST00000377685.9:c.*2448-32G>C	ENSP00000366913.4:n.*2448-32G>C
ENST00000539276.6:c.2608-32G>C	ENSP00000440045.2:n.2608-32G>C
ENST00000547792.1:n.511G>C
ENST00000548169.2:c.2279-32G>C
NM_001681.3:c.2608-32G>C	NP_001672.1:n.2608-32G>C
NM_170665.3:c.2608-32G>C	NP_733765.1:n.2608-32G>C
XM_005253888.1:c.2608-32G>C	XP_005253945.1:n.2608-32G>C
XM_011538402.1:c.2608-32G>C	XP_011536704.1:n.2608-32G>C
XR_243009.1:n.2614-32G>C
XM_005253888.3:c.2608-32G>C	XP_005253945.1:n.2608-32G>C
XM_011538402.3:c.2608-32G>C	XP_011536704.1:n.2608-32G>C
XR_002957329.1:n.2614-32G>C
XR_243009.3:n.2614-32G>C
NM_170665.4:c.2608-32G>C MANE Select	NP_733765.1:n.2608-32G>C
NM_001681.4:c.2608-32G>C	NP_001672.1:n.2608-32G>C