Canonical Allele Identifier: CA437316367

Gene: KCNMB3

Linked Data

• MyVariant Identifiers: chr3:g.178960788G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179243000G>C , CM000665.2:g.179243000G>C	GRCh38
NC_000003.11:g.178960788G>C , CM000665.1:g.178960788G>C	GRCh37
NC_000003.10:g.180443482G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392685.7:c.732C>G MANE Select	ENSP00000376451.2:p.Val244=
ENST00000314235.9:c.744C>G	ENSP00000319370.5:p.Val248=
ENST00000349697.2:c.738C>G	ENSP00000327866.2:p.Val246=
ENST00000392685.6:c.732C>G	ENSP00000376451.2:p.Val244=
ENST00000392686.6:c.678C>G	ENSP00000376452.2:p.Val226=
ENST00000485523.5:c.678C>G	ENSP00000418536.1:p.Val226=
ENST00000486944.2:c.152+133C>G	ENSP00000479162.1:n.152+133C>G
ENST00000497599.5:c.453+1495C>G	ENSP00000417091.1:n.453+1495C>G
NM_001163677.1:c.453+1495C>G	NP_001157149.1:n.453+1495C>G
NM_014407.3:c.744C>G	NP_055222.3:p.Val248=
NM_171828.2:c.738C>G	NP_741979.1:p.Val246=
NM_171829.2:c.678C>G	NP_741980.1:p.Val226=
NM_171830.1:c.732C>G	NP_741981.1:p.Val244=
NR_028135.1:n.1620C>G
NM_001163677.2:c.453+1495C>G	NP_001157149.1:n.453+1495C>G
NM_171828.3:c.738C>G	NP_741979.1:p.Val246=
NM_171829.3:c.678C>G	NP_741980.1:p.Val226=
NR_028135.2:n.1620C>G
NM_171830.2:c.732C>G MANE Select	NP_741981.1:p.Val244=