Canonical Allele Identifier: CA2670598949

Gene: SGCB

Linked Data

• gnomAD v4: 4-52028710-ACAAAGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028714_52028719del , CM000666.2:g.52028714_52028719del	GRCh38
NC_000004.11:g.52894880_52894885del , CM000666.1:g.52894880_52894885del	GRCh37
NC_000004.10:g.52589637_52589642del	NCBI36
NG_008891.1:g.14604_14609del , LRG_204:g.14604_14609del

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.621+14_621+19del MANE Select	ENSP00000370839.6:n.621+14_621+19del
ENST00000381431.9:c.621+14_621+19del	ENSP00000370839.5:n.621+14_621+19del
NM_000232.4:c.621+14_621+19del , LRG_204t1:c.621+14_621+19del	NP_000223.1:n.621+14_621+19del
XM_006714049.2:c.324+14_324+19del	XP_006714112.1:n.324+14_324+19del
XM_011534403.1:c.411+14_411+19del	XP_011532705.1:n.411+14_411+19del
XM_011534404.1:c.324+14_324+19del	XP_011532706.1:n.324+14_324+19del
NM_000232.5:c.621+14_621+19del MANE Select	NP_000223.1:n.621+14_621+19del