Canonical Allele Identifier: CA382777447

Gene: SCN4B

Linked Data

• dbSNP Id: rs1555097088
• MyVariant Identifiers: chr11:g.118011941T>A (hg19) ; chr11:g.118141226T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141226T>A , CM000673.2:g.118141226T>A	GRCh38
NC_000011.9:g.118011941T>A , CM000673.1:g.118011941T>A	GRCh37
NC_000011.8:g.117517151T>A	NCBI36
NG_011710.1:g.16690A>T , LRG_330:g.16690A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.574A>T MANE Select	ENSP00000322460.4:p.Lys192Ter
ENST00000324727.8:c.574A>T	ENSP00000322460.4:p.Lys192Ter
ENST00000415030.6:n.717A>T
ENST00000423160.2:n.208A>T
ENST00000529878.1:c.172A>T	ENSP00000436343.1:p.Lys58Ter
ENST00000531550.1:n.639A>T
ENST00000532138.1:n.830A>T
NM_001142348.1:c.172A>T	NP_001135820.1:p.Lys58Ter
NM_001142349.1:c.244A>T	NP_001135821.1:p.Lys82Ter
NM_174934.3:c.574A>T , LRG_330t1:c.574A>T	NP_777594.1:p.Lys192Ter
NR_024527.1:n.599A>T
NM_001142348.2:c.172A>T	NP_001135820.1:p.Lys58Ter
NM_001142349.2:c.244A>T	NP_001135821.1:p.Lys82Ter
NR_024527.2:n.563A>T
NM_174934.4:c.574A>T MANE Select	NP_777594.1:p.Lys192Ter