Canonical Allele Identifier: CA6299961

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118134075C>T , CM000673.2:g.118134075C>T	GRCh38
NC_000011.9:g.118004790C>T , CM000673.1:g.118004790C>T	GRCh37
NC_000011.8:g.117510000C>T	NCBI36
NG_011710.1:g.23841G>A , LRG_330:g.23841G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.*2952G>A MANE Select	ENSP00000322460.4:n.*2952G>A
ENST00000324727.8:c.*2952G>A	ENSP00000322460.4:n.*2952G>A
ENST00000415030.6:n.3782G>A
ENST00000423160.2:n.3273G>A
NM_001142348.1:c.*2952G>A	NP_001135820.1:n.*2952G>A
NM_001142349.1:c.*2952G>A	NP_001135821.1:n.*2952G>A
NM_174934.3:c.*2952G>A , LRG_330t1:c.*2952G>A	NP_777594.1:n.*2952G>A
NR_024527.1:n.3664G>A
NM_001142348.2:c.*2952G>A	NP_001135820.1:n.*2952G>A
NM_001142349.2:c.*2952G>A	NP_001135821.1:n.*2952G>A
NR_024527.2:n.3628G>A
NM_174934.4:c.*2952G>A MANE Select	NP_777594.1:n.*2952G>A