Canonical Allele Identifier: CA15290306
Gene: KCNMB2 HGNC NCBI
KCNMB2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.178623794G>A , CM000665.2:g.178623794G>A GRCh38
NC_000003.11:g.178341582G>A , CM000665.1:g.178341582G>A GRCh37
NC_000003.10:g.179824276G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000452583.6:c.-68+87083G>A (KCNMB2) MANE Select ENSP00000397483.1:n.-68+87083G>A
ENST00000420517.6:c.-145+87083G>A (KCNMB2) ENSP00000408252.2:n.-145+87083G>A
ENST00000422927.1:c.-68+64810G>A (KCNMB2) ENSP00000414228.1:n.-68+64810G>A
ENST00000432997.5:c.-68+64810G>A (KCNMB2) ENSP00000407592.1:n.-68+64810G>A
ENST00000437510.5:c.-67-183549G>A (KCNMB2) ENSP00000395807.1:n.-67-183549G>A
ENST00000452583.5:c.-68+87083G>A (KCNMB2) ENSP00000397483.1:n.-68+87083G>A
ENST00000455865.5:c.-145+64810G>A (KCNMB2) ENSP00000399100.1:n.-145+64810G>A
ENST00000470361.6:n.476+87083G>A (KCNMB2)
ENST00000614557.1:c.-67-183549G>A ENSP00000483415.1:n.-67-183549G>A
NM_001278911.1:c.-68+64810G>A (KCNMB2) NP_001265840.1:n.-68+64810G>A
NM_005832.4:c.-145+64810G>A (KCNMB2) NP_005823.1:n.-145+64810G>A
NM_181361.2:c.-68+87083G>A (KCNMB2) NP_852006.1:n.-68+87083G>A
NR_126560.1:n.575-86398C>T (KCNMB2-AS1)
NR_126561.1:n.638-97169C>T (KCNMB2-AS1)
XM_011512325.1:c.-145+87083G>A (KCNMB2) XP_011510627.1:n.-145+87083G>A
XM_011512326.1:c.-220+87083G>A (KCNMB2) XP_011510628.1:n.-220+87083G>A
XM_011512327.1:c.-220+64810G>A (KCNMB2) XP_011510629.1:n.-220+64810G>A
XM_011512328.1:c.-111+64810G>A (KCNMB2) XP_011510630.1:n.-111+64810G>A
XM_011512325.2:c.-145+87083G>A (KCNMB2) XP_011510627.1:n.-145+87083G>A
NM_181361.3:c.-68+87083G>A (KCNMB2) MANE Select NP_852006.1:n.-68+87083G>A
NM_001278911.2:c.-68+64810G>A (KCNMB2) NP_001265840.1:n.-68+64810G>A
NM_005832.5:c.-145+64810G>A (KCNMB2) NP_005823.1:n.-145+64810G>A