Canonical Allele Identifier: CA2003367964

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141413T= , CM000673.2:g.118141413T=	GRCh38
NC_000011.9:g.118012128T= , CM000673.1:g.118012128T=	GRCh37
NC_000011.8:g.117517338T=	NCBI36
NG_011710.1:g.16503A= , LRG_330:g.16503A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.464-77A= MANE Select	ENSP00000322460.4:n.464-77A=
ENST00000324727.8:c.464-77A=	ENSP00000322460.4:n.464-77A=
ENST00000415030.6:n.607-77A=
ENST00000423160.2:n.98-77A=
ENST00000529878.1:c.62-77A=	ENSP00000436343.1:n.62-77A=
ENST00000531550.1:n.452A=
ENST00000532138.1:n.720-77A=
NM_001142348.1:c.62-77A=	NP_001135820.1:n.62-77A=
NM_001142349.1:c.134-77A=	NP_001135821.1:n.134-77A=
NM_174934.3:c.464-77A= , LRG_330t1:c.464-77A=	NP_777594.1:n.464-77A=
NR_024527.1:n.489-77A=
NM_001142348.2:c.62-77A=	NP_001135820.1:n.62-77A=
NM_001142349.2:c.134-77A=	NP_001135821.1:n.134-77A=
NR_024527.2:n.453-77A=
NM_174934.4:c.464-77A= MANE Select	NP_777594.1:n.464-77A=