Canonical Allele Identifier: CA2670598608

Gene: SGCB

Linked Data

• gnomAD v4: 4-52027911-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52027913del , CM000666.2:g.52027913del	GRCh38
NC_000004.11:g.52894079del , CM000666.1:g.52894079del	GRCh37
NC_000004.10:g.52588836del	NCBI36
NG_008891.1:g.15408del , LRG_204:g.15408del

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.753+56del MANE Select	ENSP00000370839.6:n.753+56del
ENST00000381431.9:c.753+56del	ENSP00000370839.5:n.753+56del
NM_000232.4:c.753+56del , LRG_204t1:c.753+56del	NP_000223.1:n.753+56del
XM_006714049.2:c.456+56del	XP_006714112.1:n.456+56del
XM_011534403.1:c.543+56del	XP_011532705.1:n.543+56del
XM_011534404.1:c.456+56del	XP_011532706.1:n.456+56del
NM_000232.5:c.753+56del MANE Select	NP_000223.1:n.753+56del