Canonical Allele Identifier: CA2670614642

Gene: SGCB

Linked Data

• gnomAD v4: 4-52038262-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52038264_52038265del , CM000666.2:g.52038264_52038265del	GRCh38
NC_000004.11:g.52904430_52904431del , CM000666.1:g.52904430_52904431del	GRCh37
NC_000004.10:g.52599187_52599188del	NCBI36
NG_008891.1:g.5056_5057del , LRG_204:g.5056_5057del

Transcript Alleles

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