Canonical Allele Identifier: CA2003369041
Gene: SCN4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118143924G= , CM000673.2:g.118143924G= GRCh38
NC_000011.9:g.118014639G= , CM000673.1:g.118014639G= GRCh37
NC_000011.8:g.117519849G= NCBI36
NG_011710.1:g.13992C= , LRG_330:g.13992C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324727.9:c.372C= MANE Select ENSP00000322460.4:p.Ser124=
ENST00000324727.8:c.372C= ENSP00000322460.4:p.Ser124=
ENST00000415030.6:n.515C=
ENST00000529878.1:c.62-2588C= ENSP00000436343.1:n.62-2588C=
ENST00000532138.1:n.719+63C=
NM_001142348.1:c.62-2588C= NP_001135820.1:n.62-2588C=
NM_001142349.1:c.42C= NP_001135821.1:p.Ser14=
NM_174934.3:c.372C= , LRG_330t1:c.372C= NP_777594.1:p.Ser124=
NR_024527.1:n.488+63C=
NM_001142348.2:c.62-2588C= NP_001135820.1:n.62-2588C=
NM_001142349.2:c.42C= NP_001135821.1:p.Ser14=
NR_024527.2:n.452+63C=
NM_174934.4:c.372C= MANE Select NP_777594.1:p.Ser124=