Canonical Allele Identifier: CA355288497

Gene: KCNMB3

Linked Data

• MyVariant Identifiers: chr3:g.178960849A>G (hg19) ; chr3:g.179243061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179243061A>G , CM000665.2:g.179243061A>G	GRCh38
NC_000003.11:g.178960849A>G , CM000665.1:g.178960849A>G	GRCh37
NC_000003.10:g.180443543A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392685.7:c.671T>C MANE Select	ENSP00000376451.2:p.Val224Ala
ENST00000314235.9:c.683T>C	ENSP00000319370.5:p.Val228Ala
ENST00000349697.2:c.677T>C	ENSP00000327866.2:p.Val226Ala
ENST00000392685.6:c.671T>C	ENSP00000376451.2:p.Val224Ala
ENST00000392686.6:c.617T>C	ENSP00000376452.2:p.Val206Ala
ENST00000485523.5:c.617T>C	ENSP00000418536.1:p.Val206Ala
ENST00000486944.2:c.152+72T>C	ENSP00000479162.1:n.152+72T>C
ENST00000497599.5:c.453+1434T>C	ENSP00000417091.1:n.453+1434T>C
NM_001163677.1:c.453+1434T>C	NP_001157149.1:n.453+1434T>C
NM_014407.3:c.683T>C	NP_055222.3:p.Val228Ala
NM_171828.2:c.677T>C	NP_741979.1:p.Val226Ala
NM_171829.2:c.617T>C	NP_741980.1:p.Val206Ala
NM_171830.1:c.671T>C	NP_741981.1:p.Val224Ala
NR_028135.1:n.1559T>C
NM_001163677.2:c.453+1434T>C	NP_001157149.1:n.453+1434T>C
NM_171828.3:c.677T>C	NP_741979.1:p.Val226Ala
NM_171829.3:c.617T>C	NP_741980.1:p.Val206Ala
NR_028135.2:n.1559T>C
NM_171830.2:c.671T>C MANE Select	NP_741981.1:p.Val224Ala