Canonical Allele Identifier: CA10698199
Gene: ATP2B4 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.203682799T>C
GRCh37 chr1:g.203651927T>C
gnomAD v2:
1:203651927 T / C
gnomAD v3:
1:203682799 T / C
gnomAD v4:
chr1-203682799-T-C
Joint Max Group AF 0.97679464 (EAS)
Genomes Max Group AF 0.97645512 (EAS)
Exomes Max Group AF 0.86874173 (EAS)
dbSNP:
1541252
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.203682799T>C , CM000663.2:g.203682799T>C GRCh38
NC_000001.10:g.203651927T>C , CM000663.1:g.203651927T>C GRCh37
NC_000001.9:g.201918550T>C NCBI36
NG_029589.1:g.61013T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000341360.7:c.-407T>C ENSP00000340930.2:n.-407T>C
ENST00000705901.1:c.-407T>C ENSP00000516177.1:n.-407T>C
ENST00000357681.10:c.-407T>C MANE Select ENSP00000350310.5:n.-407T>C
ENST00000357681.9:c.-407T>C ENSP00000350310.5:n.-407T>C
ENST00000367218.7:c.-407T>C ENSP00000356187.3:n.-407T>C
NM_001001396.2:c.-407T>C NP_001001396.1:n.-407T>C
NM_001684.4:c.-407T>C NP_001675.3:n.-407T>C
NM_001365783.1:c.-407T>C NP_001352712.1:n.-407T>C
NM_001365784.1:c.-407T>C NP_001352713.1:n.-407T>C
NM_001365783.2:c.-407T>C NP_001352712.1:n.-407T>C
NM_001684.5:c.-407T>C MANE Select NP_001675.3:n.-407T>C
NM_001001396.3:c.-407T>C NP_001001396.1:n.-407T>C
NM_001365784.2:c.-407T>C NP_001352713.1:n.-407T>C
Search 100 bp 5'
Search 100 bp 3'