Canonical Allele Identifier: CA1457429066

Gene: SGCB

Linked Data

• dbSNP Id: rs1737141447

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52027867_52027868del , CM000666.2:g.52027867_52027868del	GRCh38
NC_000004.11:g.52894033_52894034del , CM000666.1:g.52894033_52894034del	GRCh37
NC_000004.10:g.52588790_52588791del	NCBI36
NG_008891.1:g.15453_15454del , LRG_204:g.15453_15454del

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.753+101_753+102del MANE Select	ENSP00000370839.6:n.753+101_753+102del
ENST00000381431.9:c.753+101_753+102del	ENSP00000370839.5:n.753+101_753+102del
NM_000232.4:c.753+101_753+102del , LRG_204t1:c.753+101_753+102del	NP_000223.1:n.753+101_753+102del
XM_006714049.2:c.456+101_456+102del	XP_006714112.1:n.456+101_456+102del
XM_011534403.1:c.543+101_543+102del	XP_011532705.1:n.543+101_543+102del
XM_011534404.1:c.456+101_456+102del	XP_011532706.1:n.456+101_456+102del
NM_000232.5:c.753+101_753+102del MANE Select	NP_000223.1:n.753+101_753+102del