Canonical Allele Identifier: CA2838392735
Gene: ATP2B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10698992T>G , CM000665.2:g.10698992T>G GRCh38
NC_000003.11:g.10740677T>G , CM000665.1:g.10740677T>G GRCh37
NC_000003.10:g.10715677T>G NCBI36
NG_012046.2:g.14040A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646379.1:c.-460+8923A>C ENSP00000494381.1:n.-460+8923A>C
ENST00000397077.5:c.-460+8923A>C ENSP00000380267.1:n.-460+8923A>C
XM_006713175.2:c.-460+8923A>C XP_006713238.1:n.-460+8923A>C
XM_011533751.1:c.-556+8923A>C XP_011532053.1:n.-556+8923A>C
XM_006713175.4:c.-460+8923A>C XP_006713238.1:n.-460+8923A>C
XM_017006484.2:c.-460+8923A>C XP_016861973.1:n.-460+8923A>C
XM_017006487.1:c.-460+8923A>C XP_016861976.1:n.-460+8923A>C