Canonical Allele Identifier: CA355288523

Gene: KCNMB3

Linked Data

• MyVariant Identifiers: chr3:g.178960864C>A (hg19) ; chr3:g.179243076C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179243076C>A , CM000665.2:g.179243076C>A	GRCh38
NC_000003.11:g.178960864C>A , CM000665.1:g.178960864C>A	GRCh37
NC_000003.10:g.180443558C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392685.7:c.656G>T MANE Select	ENSP00000376451.2:p.Gly219Val
ENST00000314235.9:c.668G>T	ENSP00000319370.5:p.Gly223Val
ENST00000349697.2:c.662G>T	ENSP00000327866.2:p.Gly221Val
ENST00000392685.6:c.656G>T	ENSP00000376451.2:p.Gly219Val
ENST00000392686.6:c.602G>T	ENSP00000376452.2:p.Gly201Val
ENST00000485523.5:c.602G>T	ENSP00000418536.1:p.Gly201Val
ENST00000486944.2:c.152+57G>T	ENSP00000479162.1:n.152+57G>T
ENST00000497599.5:c.453+1419G>T	ENSP00000417091.1:n.453+1419G>T
NM_001163677.1:c.453+1419G>T	NP_001157149.1:n.453+1419G>T
NM_014407.3:c.668G>T	NP_055222.3:p.Gly223Val
NM_171828.2:c.662G>T	NP_741979.1:p.Gly221Val
NM_171829.2:c.602G>T	NP_741980.1:p.Gly201Val
NM_171830.1:c.656G>T	NP_741981.1:p.Gly219Val
NR_028135.1:n.1544G>T
NM_001163677.2:c.453+1419G>T	NP_001157149.1:n.453+1419G>T
NM_171828.3:c.662G>T	NP_741979.1:p.Gly221Val
NM_171829.3:c.602G>T	NP_741980.1:p.Gly201Val
NR_028135.2:n.1544G>T
NM_171830.2:c.656G>T MANE Select	NP_741981.1:p.Gly219Val