Canonical Allele Identifier: CA1341772
Gene: ATP2B4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
COSMIC:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203711957T>C , CM000663.2:g.203711957T>C GRCh38
NC_000001.10:g.203681085T>C , CM000663.1:g.203681085T>C GRCh37
NC_000001.9:g.201947708T>C NCBI36
NG_029589.1:g.90171T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000341360.7:c.2032-3T>C ENSP00000340930.2:n.2032-3T>C
ENST00000705901.1:c.1996-3T>C ENSP00000516177.1:n.1996-3T>C
ENST00000357681.10:c.2032-3T>C MANE Select ENSP00000350310.5:n.2032-3T>C
ENST00000341360.6:c.2032-3T>C ENSP00000340930.2:n.2032-3T>C
ENST00000357681.9:c.2032-3T>C ENSP00000350310.5:n.2032-3T>C
ENST00000367218.7:c.2032-3T>C ENSP00000356187.3:n.2032-3T>C
NM_001001396.2:c.2032-3T>C NP_001001396.1:n.2032-3T>C
NM_001684.4:c.2032-3T>C NP_001675.3:n.2032-3T>C
NM_001365783.1:c.2032-3T>C NP_001352712.1:n.2032-3T>C
NM_001365784.1:c.2032-3T>C NP_001352713.1:n.2032-3T>C
NM_001365783.2:c.2032-3T>C NP_001352712.1:n.2032-3T>C
NM_001684.5:c.2032-3T>C MANE Select NP_001675.3:n.2032-3T>C
NM_001001396.3:c.2032-3T>C NP_001001396.1:n.2032-3T>C
NM_001365784.2:c.2032-3T>C NP_001352713.1:n.2032-3T>C