Canonical Allele Identifier: CA2574993157

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141405T>C , CM000673.2:g.118141405T>C	GRCh38
NC_000011.9:g.118012120T>C , CM000673.1:g.118012120T>C	GRCh37
NC_000011.8:g.117517330T>C	NCBI36
NG_011710.1:g.16511A>G , LRG_330:g.16511A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.464-69A>G MANE Select	ENSP00000322460.4:n.464-69A>G
ENST00000324727.8:c.464-69A>G	ENSP00000322460.4:n.464-69A>G
ENST00000415030.6:n.607-69A>G
ENST00000423160.2:n.98-69A>G
ENST00000529878.1:c.62-69A>G	ENSP00000436343.1:n.62-69A>G
ENST00000531550.1:n.460A>G
ENST00000532138.1:n.720-69A>G
NM_001142348.1:c.62-69A>G	NP_001135820.1:n.62-69A>G
NM_001142349.1:c.134-69A>G	NP_001135821.1:n.134-69A>G
NM_174934.3:c.464-69A>G , LRG_330t1:c.464-69A>G	NP_777594.1:n.464-69A>G
NR_024527.1:n.489-69A>G
NM_001142348.2:c.62-69A>G	NP_001135820.1:n.62-69A>G
NM_001142349.2:c.134-69A>G	NP_001135821.1:n.134-69A>G
NR_024527.2:n.453-69A>G
NM_174934.4:c.464-69A>G MANE Select	NP_777594.1:n.464-69A>G