Canonical Allele Identifier: CA2670598952

Gene: SGCB

Linked Data

• gnomAD v4: 4-52028718-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028718A>C , CM000666.2:g.52028718A>C	GRCh38
NC_000004.11:g.52894884A>C , CM000666.1:g.52894884A>C	GRCh37
NC_000004.10:g.52589641A>C	NCBI36
NG_008891.1:g.14602T>G , LRG_204:g.14602T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.621+12T>G MANE Select	ENSP00000370839.6:n.621+12T>G
ENST00000381431.9:c.621+12T>G	ENSP00000370839.5:n.621+12T>G
NM_000232.4:c.621+12T>G , LRG_204t1:c.621+12T>G	NP_000223.1:n.621+12T>G
XM_006714049.2:c.324+12T>G	XP_006714112.1:n.324+12T>G
XM_011534403.1:c.411+12T>G	XP_011532705.1:n.411+12T>G
XM_011534404.1:c.324+12T>G	XP_011532706.1:n.324+12T>G
NM_000232.5:c.621+12T>G MANE Select	NP_000223.1:n.621+12T>G