Canonical Allele Identifier: CA2670614139

Gene: SGCB

Linked Data

• gnomAD v4: 4-52033363-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52033363G>T , CM000666.2:g.52033363G>T	GRCh38
NC_000004.11:g.52899529G>T , CM000666.1:g.52899529G>T	GRCh37
NC_000004.10:g.52594286G>T	NCBI36
NG_008891.1:g.9957C>A , LRG_204:g.9957C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.243+68C>A MANE Select	ENSP00000370839.6:n.243+68C>A
ENST00000381431.9:c.243+68C>A	ENSP00000370839.5:n.243+68C>A
ENST00000506357.5:c.229+68C>A
ENST00000514133.1:c.210+68C>A	ENSP00000425818.1:n.210+68C>A
NM_000232.4:c.243+68C>A , LRG_204t1:c.243+68C>A	NP_000223.1:n.243+68C>A
XM_006714049.2:c.-165+68C>A	XP_006714112.1:n.-165+68C>A
XM_011534403.1:c.34-3500C>A	XP_011532705.1:n.34-3500C>A
XM_011534404.1:c.-142+68C>A	XP_011532706.1:n.-142+68C>A
NM_000232.5:c.243+68C>A MANE Select	NP_000223.1:n.243+68C>A