Canonical Allele Identifier: CA2003366031
Gene: SCN4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118137118T= , CM000673.2:g.118137118T= GRCh38
NC_000011.9:g.118007833T= , CM000673.1:g.118007833T= GRCh37
NC_000011.8:g.117513043T= NCBI36
NG_011710.1:g.20798A= , LRG_330:g.20798A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324727.9:c.596A= MANE Select ENSP00000322460.4:p.Lys199=
ENST00000324727.8:c.596A= ENSP00000322460.4:p.Lys199=
ENST00000415030.6:n.739A=
ENST00000423160.2:n.230A=
ENST00000529878.1:c.194A= ENSP00000436343.1:p.Lys65=
ENST00000531550.1:n.661A=
NM_001142348.1:c.194A= NP_001135820.1:p.Lys65=
NM_001142349.1:c.266A= NP_001135821.1:p.Lys89=
NM_174934.3:c.596A= , LRG_330t1:c.596A= NP_777594.1:p.Lys199=
NR_024527.1:n.621A=
NM_001142348.2:c.194A= NP_001135820.1:p.Lys65=
NM_001142349.2:c.266A= NP_001135821.1:p.Lys89=
NR_024527.2:n.585A=
NM_174934.4:c.596A= MANE Select NP_777594.1:p.Lys199=