Canonical Allele Identifier: CA437316428

Gene: KCNMB3

Linked Data

• MyVariant Identifiers: chr3:g.178960863A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179243075A>T , CM000665.2:g.179243075A>T	GRCh38
NC_000003.11:g.178960863A>T , CM000665.1:g.178960863A>T	GRCh37
NC_000003.10:g.180443557A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392685.7:c.657T>A MANE Select	ENSP00000376451.2:p.Gly219=
ENST00000314235.9:c.669T>A	ENSP00000319370.5:p.Gly223=
ENST00000349697.2:c.663T>A	ENSP00000327866.2:p.Gly221=
ENST00000392685.6:c.657T>A	ENSP00000376451.2:p.Gly219=
ENST00000392686.6:c.603T>A	ENSP00000376452.2:p.Gly201=
ENST00000485523.5:c.603T>A	ENSP00000418536.1:p.Gly201=
ENST00000486944.2:c.152+58T>A	ENSP00000479162.1:n.152+58T>A
ENST00000497599.5:c.453+1420T>A	ENSP00000417091.1:n.453+1420T>A
NM_001163677.1:c.453+1420T>A	NP_001157149.1:n.453+1420T>A
NM_014407.3:c.669T>A	NP_055222.3:p.Gly223=
NM_171828.2:c.663T>A	NP_741979.1:p.Gly221=
NM_171829.2:c.603T>A	NP_741980.1:p.Gly201=
NM_171830.1:c.657T>A	NP_741981.1:p.Gly219=
NR_028135.1:n.1545T>A
NM_001163677.2:c.453+1420T>A	NP_001157149.1:n.453+1420T>A
NM_171828.3:c.663T>A	NP_741979.1:p.Gly221=
NM_171829.3:c.603T>A	NP_741980.1:p.Gly201=
NR_028135.2:n.1545T>A
NM_171830.2:c.657T>A MANE Select	NP_741981.1:p.Gly219=