Canonical Allele Identifier: CA2670614648

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038265-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038266del , CM000666.2:g.52038266del	GRCh38
NC_000004.11:g.52904432del , CM000666.1:g.52904432del	GRCh37
NC_000004.10:g.52599189del	NCBI36
NG_008891.1:g.5054del , LRG_204:g.5054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.-7del MANE Select	ENSP00000370839.6:n.-7del
ENST00000381431.9:c.-7del	ENSP00000370839.5:n.-7del
NM_000232.4:c.-7del , LRG_204t1:c.-7del	NP_000223.1:n.-7del
XM_011534403.1:c.-7del	XP_011532705.1:n.-7del
NM_000232.5:c.-7del MANE Select	NP_000223.1:n.-7del