Canonical Allele Identifier: CA2003366033
Gene: SCN4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118137120C= , CM000673.2:g.118137120C= GRCh38
NC_000011.9:g.118007835C= , CM000673.1:g.118007835C= GRCh37
NC_000011.8:g.117513045C= NCBI36
NG_011710.1:g.20796G= , LRG_330:g.20796G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324727.9:c.594G= MANE Select ENSP00000322460.4:p.Lys198=
ENST00000324727.8:c.594G= ENSP00000322460.4:p.Lys198=
ENST00000415030.6:n.737G=
ENST00000423160.2:n.228G=
ENST00000529878.1:c.192G= ENSP00000436343.1:p.Lys64=
ENST00000531550.1:n.659G=
NM_001142348.1:c.192G= NP_001135820.1:p.Lys64=
NM_001142349.1:c.264G= NP_001135821.1:p.Lys88=
NM_174934.3:c.594G= , LRG_330t1:c.594G= NP_777594.1:p.Lys198=
NR_024527.1:n.619G=
NM_001142348.2:c.192G= NP_001135820.1:p.Lys64=
NM_001142349.2:c.264G= NP_001135821.1:p.Lys88=
NR_024527.2:n.583G=
NM_174934.4:c.594G= MANE Select NP_777594.1:p.Lys198=