Canonical Allele Identifier: CA382777925

Gene: SCN4B

Linked Data

• MyVariant Identifiers: chr11:g.118014586T>G (hg19) ; chr11:g.118143871T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143871T>G , CM000673.2:g.118143871T>G	GRCh38
NC_000011.9:g.118014586T>G , CM000673.1:g.118014586T>G	GRCh37
NC_000011.8:g.117519796T>G	NCBI36
NG_011710.1:g.14045A>C , LRG_330:g.14045A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.425A>C MANE Select	ENSP00000322460.4:p.Gln142Pro
ENST00000324727.8:c.425A>C	ENSP00000322460.4:p.Gln142Pro
ENST00000415030.6:n.568A>C
ENST00000529878.1:c.62-2535A>C	ENSP00000436343.1:n.62-2535A>C
ENST00000532138.1:n.719+116A>C
NM_001142348.1:c.62-2535A>C	NP_001135820.1:n.62-2535A>C
NM_001142349.1:c.95A>C	NP_001135821.1:p.Gln32Pro
NM_174934.3:c.425A>C , LRG_330t1:c.425A>C	NP_777594.1:p.Gln142Pro
NR_024527.1:n.488+116A>C
NM_001142348.2:c.62-2535A>C	NP_001135820.1:n.62-2535A>C
NM_001142349.2:c.95A>C	NP_001135821.1:p.Gln32Pro
NR_024527.2:n.452+116A>C
NM_174934.4:c.425A>C MANE Select	NP_777594.1:p.Gln142Pro