Canonical Allele Identifier: CA355288439
Gene: KCNMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179243032A>G , CM000665.2:g.179243032A>G GRCh38
NC_000003.11:g.178960820A>G , CM000665.1:g.178960820A>G GRCh37
NC_000003.10:g.180443514A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392685.7:c.700T>C MANE Select ENSP00000376451.2:p.Ser234Pro
ENST00000314235.9:c.712T>C ENSP00000319370.5:p.Ser238Pro
ENST00000349697.2:c.706T>C ENSP00000327866.2:p.Ser236Pro
ENST00000392685.6:c.700T>C ENSP00000376451.2:p.Ser234Pro
ENST00000392686.6:c.646T>C ENSP00000376452.2:p.Ser216Pro
ENST00000485523.5:c.646T>C ENSP00000418536.1:p.Ser216Pro
ENST00000486944.2:c.152+101T>C ENSP00000479162.1:n.152+101T>C
ENST00000497599.5:c.453+1463T>C ENSP00000417091.1:n.453+1463T>C
NM_001163677.1:c.453+1463T>C NP_001157149.1:n.453+1463T>C
NM_014407.3:c.712T>C NP_055222.3:p.Ser238Pro
NM_171828.2:c.706T>C NP_741979.1:p.Ser236Pro
NM_171829.2:c.646T>C NP_741980.1:p.Ser216Pro
NM_171830.1:c.700T>C NP_741981.1:p.Ser234Pro
NR_028135.1:n.1588T>C
NM_001163677.2:c.453+1463T>C NP_001157149.1:n.453+1463T>C
NM_171828.3:c.706T>C NP_741979.1:p.Ser236Pro
NM_171829.3:c.646T>C NP_741980.1:p.Ser216Pro
NR_028135.2:n.1588T>C
NM_171830.2:c.700T>C MANE Select NP_741981.1:p.Ser234Pro