Canonical Allele Identifier: CA602138460

Gene: SCN4B

Linked Data

• dbSNP Id: rs1221590694
• gnomAD v2: 11-118014542-G-A
• gnomAD v3: 11-118143827-G-A
• gnomAD v4: 11-118143827-G-A
• MyVariant Identifiers: chr11:g.118014542G>A (hg19) ; chr11:g.118143827G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143827G>A , CM000673.2:g.118143827G>A	GRCh38
NC_000011.9:g.118014542G>A , CM000673.1:g.118014542G>A	GRCh37
NC_000011.8:g.117519752G>A	NCBI36
NG_011710.1:g.14089C>T , LRG_330:g.14089C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.463+6C>T MANE Select	ENSP00000322460.4:n.463+6C>T
ENST00000324727.8:c.463+6C>T	ENSP00000322460.4:n.463+6C>T
ENST00000415030.6:n.606+6C>T
ENST00000529878.1:c.62-2491C>T	ENSP00000436343.1:n.62-2491C>T
ENST00000532138.1:n.719+160C>T
NM_001142348.1:c.62-2491C>T	NP_001135820.1:n.62-2491C>T
NM_001142349.1:c.133+6C>T	NP_001135821.1:n.133+6C>T
NM_174934.3:c.463+6C>T , LRG_330t1:c.463+6C>T	NP_777594.1:n.463+6C>T
NR_024527.1:n.488+160C>T
NM_001142348.2:c.62-2491C>T	NP_001135820.1:n.62-2491C>T
NM_001142349.2:c.133+6C>T	NP_001135821.1:n.133+6C>T
NR_024527.2:n.452+160C>T
NM_174934.4:c.463+6C>T MANE Select	NP_777594.1:n.463+6C>T