Canonical Allele Identifier: CA2005866107

Gene: SCN3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123638288A= , CM000673.2:g.123638288A=	GRCh38
NC_000011.9:g.123508996A= , CM000673.1:g.123508996A=	GRCh37
NC_000011.8:g.123014206A=	NCBI36
NG_016283.1:g.21320T= , LRG_421:g.21320T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299333.8:c.482T= MANE Select	ENSP00000299333.3:p.Met161=
ENST00000655686.1:n.325T=
ENST00000657123.1:c.482T=	ENSP00000499439.1:p.Met161=
ENST00000657191.1:c.482T=	ENSP00000499755.1:p.Met161=
ENST00000659826.1:c.231T=
ENST00000667790.1:c.*463T=	ENSP00000499234.1:n.*463T=
ENST00000299333.7:c.482T=	ENSP00000299333.3:p.Met161=
ENST00000392770.6:c.482T=	ENSP00000376523.2:p.Met161=
ENST00000527125.1:n.2837T=
ENST00000530277.5:c.482T=	ENSP00000432785.1:p.Met161=
NM_001040151.1:c.482T=	NP_001035241.1:p.Met161=
NM_018400.3:c.482T= , LRG_421t1:c.482T=	NP_060870.1:p.Met161=
XM_011542897.1:c.482T=	XP_011541199.1:p.Met161=
XR_947858.1:n.889T=
XM_011542897.2:c.482T=	XP_011541199.1:p.Met161=
NM_001040151.2:c.482T= MANE Select	NP_001035241.1:p.Met161=
NM_018400.4:c.482T=	NP_060870.1:p.Met161=