Canonical Allele Identifier: CA1457429948

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029686T= , CM000666.2:g.52029686T=	GRCh38
NC_000004.11:g.52895852T= , CM000666.1:g.52895852T=	GRCh37
NC_000004.10:g.52590609T=	NCBI36
NG_008891.1:g.13634A= , LRG_204:g.13634A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.421A= MANE Select	ENSP00000370839.6:p.Asn141=
ENST00000381431.9:c.421A=	ENSP00000370839.5:p.Asn141=
ENST00000506357.5:c.504A=
ENST00000514133.1:c.498A=	ENSP00000425818.1:n.498A=
NM_000232.4:c.421A= , LRG_204t1:c.421A=	NP_000223.1:p.Asn141=
XM_006714049.2:c.124A=	XP_006714112.1:p.Asn42=
XM_011534403.1:c.211A=	XP_011532705.1:p.Asn71=
XM_011534404.1:c.124A=	XP_011532706.1:p.Asn42=
NM_000232.5:c.421A= MANE Select	NP_000223.1:p.Asn141=