Canonical Allele Identifier: CA2536860891
Gene: SGCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038076_52038077insACC , CM000666.2:g.52038076_52038077insACC GRCh38
NC_000004.11:g.52904242_52904243insACC , CM000666.1:g.52904242_52904243insACC GRCh37
NC_000004.10:g.52598999_52599000insACC NCBI36
NG_008891.1:g.5243_5244insGGT , LRG_204:g.5243_5244insGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+150_33+151insGGT MANE Select ENSP00000370839.6:n.33+150_33+151insGGT
ENST00000381431.9:c.33+150_33+151insGGT ENSP00000370839.5:n.33+150_33+151insGGT
ENST00000506357.5:c.19+150_19+151insGGT
NM_000232.4:c.33+150_33+151insGGT , LRG_204t1:c.33+150_33+151insGGT NP_000223.1:n.33+150_33+151insGGT
XM_011534403.1:c.33+150_33+151insGGT XP_011532705.1:n.33+150_33+151insGGT
NM_000232.5:c.33+150_33+151insGGT MANE Select NP_000223.1:n.33+150_33+151insGGT