Canonical Allele Identifier: CA355288515

Gene: KCNMB3

Linked Data

• MyVariant Identifiers: chr3:g.178960858G>T (hg19) ; chr3:g.179243070G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179243070G>T , CM000665.2:g.179243070G>T	GRCh38
NC_000003.11:g.178960858G>T , CM000665.1:g.178960858G>T	GRCh37
NC_000003.10:g.180443552G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392685.7:c.662C>A MANE Select	ENSP00000376451.2:p.Ala221Asp
ENST00000314235.9:c.674C>A	ENSP00000319370.5:p.Ala225Asp
ENST00000349697.2:c.668C>A	ENSP00000327866.2:p.Ala223Asp
ENST00000392685.6:c.662C>A	ENSP00000376451.2:p.Ala221Asp
ENST00000392686.6:c.608C>A	ENSP00000376452.2:p.Ala203Asp
ENST00000485523.5:c.608C>A	ENSP00000418536.1:p.Ala203Asp
ENST00000486944.2:c.152+63C>A	ENSP00000479162.1:n.152+63C>A
ENST00000497599.5:c.453+1425C>A	ENSP00000417091.1:n.453+1425C>A
NM_001163677.1:c.453+1425C>A	NP_001157149.1:n.453+1425C>A
NM_014407.3:c.674C>A	NP_055222.3:p.Ala225Asp
NM_171828.2:c.668C>A	NP_741979.1:p.Ala223Asp
NM_171829.2:c.608C>A	NP_741980.1:p.Ala203Asp
NM_171830.1:c.662C>A	NP_741981.1:p.Ala221Asp
NR_028135.1:n.1550C>A
NM_001163677.2:c.453+1425C>A	NP_001157149.1:n.453+1425C>A
NM_171828.3:c.668C>A	NP_741979.1:p.Ala223Asp
NM_171829.3:c.608C>A	NP_741980.1:p.Ala203Asp
NR_028135.2:n.1550C>A
NM_171830.2:c.662C>A MANE Select	NP_741981.1:p.Ala221Asp