Canonical Allele Identifier: CA2616226160

Gene: SCN4B

Linked Data

• gnomAD v4: 11-118141397-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141397C>G , CM000673.2:g.118141397C>G	GRCh38
NC_000011.9:g.118012112C>G , CM000673.1:g.118012112C>G	GRCh37
NC_000011.8:g.117517322C>G	NCBI36
NG_011710.1:g.16519G>C , LRG_330:g.16519G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.464-61G>C MANE Select	ENSP00000322460.4:n.464-61G>C
ENST00000324727.8:c.464-61G>C	ENSP00000322460.4:n.464-61G>C
ENST00000415030.6:n.607-61G>C
ENST00000423160.2:n.98-61G>C
ENST00000529878.1:c.62-61G>C	ENSP00000436343.1:n.62-61G>C
ENST00000531550.1:n.468G>C
ENST00000532138.1:n.720-61G>C
NM_001142348.1:c.62-61G>C	NP_001135820.1:n.62-61G>C
NM_001142349.1:c.134-61G>C	NP_001135821.1:n.134-61G>C
NM_174934.3:c.464-61G>C , LRG_330t1:c.464-61G>C	NP_777594.1:n.464-61G>C
NR_024527.1:n.489-61G>C
NM_001142348.2:c.62-61G>C	NP_001135820.1:n.62-61G>C
NM_001142349.2:c.134-61G>C	NP_001135821.1:n.134-61G>C
NR_024527.2:n.453-61G>C
NM_174934.4:c.464-61G>C MANE Select	NP_777594.1:n.464-61G>C