Canonical Allele Identifier: CA1457429220

Gene: SGCB

Linked Data

• dbSNP Id: rs1737153255
• gnomAD v4: 4-52028207-GTTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028209_52028212del , CM000666.2:g.52028209_52028212del	GRCh38
NC_000004.11:g.52894375_52894378del , CM000666.1:g.52894375_52894378del	GRCh37
NC_000004.10:g.52589132_52589135del	NCBI36
NG_008891.1:g.15109_15112del , LRG_204:g.15109_15112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.622-112_622-109del MANE Select	ENSP00000370839.6:n.622-112_622-109del
ENST00000381431.9:c.622-112_622-109del	ENSP00000370839.5:n.622-112_622-109del
NM_000232.4:c.622-112_622-109del , LRG_204t1:c.622-112_622-109del	NP_000223.1:n.622-112_622-109del
XM_006714049.2:c.325-112_325-109del	XP_006714112.1:n.325-112_325-109del
XM_011534403.1:c.412-112_412-109del	XP_011532705.1:n.412-112_412-109del
XM_011534404.1:c.325-112_325-109del	XP_011532706.1:n.325-112_325-109del
NM_000232.5:c.622-112_622-109del MANE Select	NP_000223.1:n.622-112_622-109del