Canonical Allele Identifier: CA382777633

Gene: SCN4B

Linked Data

• MyVariant Identifiers: chr11:g.118012037T>A (hg19) ; chr11:g.118141322T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141322T>A , CM000673.2:g.118141322T>A	GRCh38
NC_000011.9:g.118012037T>A , CM000673.1:g.118012037T>A	GRCh37
NC_000011.8:g.117517247T>A	NCBI36
NG_011710.1:g.16594A>T , LRG_330:g.16594A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324727.9:c.478A>T MANE Select	ENSP00000322460.4:p.Asn160Tyr
ENST00000324727.8:c.478A>T	ENSP00000322460.4:p.Asn160Tyr
ENST00000415030.6:n.621A>T
ENST00000423160.2:n.112A>T
ENST00000529878.1:c.76A>T	ENSP00000436343.1:p.Asn26Tyr
ENST00000531550.1:n.543A>T
ENST00000532138.1:n.734A>T
NM_001142348.1:c.76A>T	NP_001135820.1:p.Asn26Tyr
NM_001142349.1:c.148A>T	NP_001135821.1:p.Asn50Tyr
NM_174934.3:c.478A>T , LRG_330t1:c.478A>T	NP_777594.1:p.Asn160Tyr
NR_024527.1:n.503A>T
NM_001142348.2:c.76A>T	NP_001135820.1:p.Asn26Tyr
NM_001142349.2:c.148A>T	NP_001135821.1:p.Asn50Tyr
NR_024527.2:n.467A>T
NM_174934.4:c.478A>T MANE Select	NP_777594.1:p.Asn160Tyr