Canonical Allele Identifier: CA11388326
Gene: KCNMB2 HGNC NCBI
KCNMB2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs13100616

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.178681763A>G , CM000665.2:g.178681763A>G GRCh38
NC_000003.11:g.178399551A>G , CM000665.1:g.178399551A>G GRCh37
NC_000003.10:g.179882245A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000452583.6:c.-67-125580A>G (KCNMB2) MANE Select ENSP00000397483.1:n.-67-125580A>G
ENST00000420517.6:c.-144-113379A>G (KCNMB2) ENSP00000408252.2:n.-144-113379A>G
ENST00000422927.1:c.-68+122779A>G (KCNMB2) ENSP00000414228.1:n.-68+122779A>G
ENST00000432997.5:c.-68+122779A>G (KCNMB2) ENSP00000407592.1:n.-68+122779A>G
ENST00000437510.5:c.-67-125580A>G (KCNMB2) ENSP00000395807.1:n.-67-125580A>G
ENST00000452583.5:c.-67-125580A>G (KCNMB2) ENSP00000397483.1:n.-67-125580A>G
ENST00000455865.5:c.-144-113379A>G (KCNMB2) ENSP00000399100.1:n.-144-113379A>G
ENST00000470361.6:n.477-125580A>G (KCNMB2)
ENST00000614557.1:c.-67-125580A>G ENSP00000483415.1:n.-67-125580A>G
NM_001278911.1:c.-68+122779A>G (KCNMB2) NP_001265840.1:n.-68+122779A>G
NM_005832.4:c.-144-113379A>G (KCNMB2) NP_005823.1:n.-144-113379A>G
NM_181361.2:c.-67-125580A>G (KCNMB2) NP_852006.1:n.-67-125580A>G
NR_126560.1:n.574+66641T>C (KCNMB2-AS1)
NR_126561.1:n.637+66666T>C (KCNMB2-AS1)
XM_011512325.1:c.-144-113379A>G (KCNMB2) XP_011510627.1:n.-144-113379A>G
XM_011512326.1:c.-219-125580A>G (KCNMB2) XP_011510628.1:n.-219-125580A>G
XM_011512327.1:c.-220+122779A>G (KCNMB2) XP_011510629.1:n.-220+122779A>G
XM_011512328.1:c.-111+122779A>G (KCNMB2) XP_011510630.1:n.-111+122779A>G
XM_011512325.2:c.-144-113379A>G (KCNMB2) XP_011510627.1:n.-144-113379A>G
NM_181361.3:c.-67-125580A>G (KCNMB2) MANE Select NP_852006.1:n.-67-125580A>G
NM_001278911.2:c.-68+122779A>G (KCNMB2) NP_001265840.1:n.-68+122779A>G
NM_005832.5:c.-144-113379A>G (KCNMB2) NP_005823.1:n.-144-113379A>G