Canonical Allele Identifier: CA477355769

Gene: SCN4B

Linked Data

• MyVariant Identifiers: chr11:g.118014552A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143837A>G , CM000673.2:g.118143837A>G	GRCh38
NC_000011.9:g.118014552A>G , CM000673.1:g.118014552A>G	GRCh37
NC_000011.8:g.117519762A>G	NCBI36
NG_011710.1:g.14079T>C , LRG_330:g.14079T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.459T>C MANE Select	ENSP00000322460.4:p.Asp153=
ENST00000324727.8:c.459T>C	ENSP00000322460.4:p.Asp153=
ENST00000415030.6:n.602T>C
ENST00000529878.1:c.62-2501T>C	ENSP00000436343.1:n.62-2501T>C
ENST00000532138.1:n.719+150T>C
NM_001142348.1:c.62-2501T>C	NP_001135820.1:n.62-2501T>C
NM_001142349.1:c.129T>C	NP_001135821.1:p.Asp43=
NM_174934.3:c.459T>C , LRG_330t1:c.459T>C	NP_777594.1:p.Asp153=
NR_024527.1:n.488+150T>C
NM_001142348.2:c.62-2501T>C	NP_001135820.1:n.62-2501T>C
NM_001142349.2:c.129T>C	NP_001135821.1:p.Asp43=
NR_024527.2:n.452+150T>C
NM_174934.4:c.459T>C MANE Select	NP_777594.1:p.Asp153=