Canonical Allele Identifier: CA1457434222
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038284_52038298delinsCTCCCCGCCCGACTG , CM000666.2:g.52038284_52038298delinsCTCCCCGCCCGACTG GRCh38
NC_000004.11:g.52904450_52904464delinsCTCCCCGCCCGACTG , CM000666.1:g.52904450_52904464delinsCTCCCCGCCCGACTG GRCh37
NC_000004.10:g.52599207_52599221delinsCTCCCCGCCCGACTG NCBI36
NG_008891.1:g.5022_5036delinsCAGTCGGGCGGGGAG , LRG_204:g.5022_5036delinsCAGTCGGGCGGGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-39_-25delinsCAGTCGGGCGGGGAG MANE Select ENSP00000370839.6:n.-39_-25delinsCAGTCGGGCGGGGAG
ENST00000381431.9:c.-39_-25delinsCAGTCGGGCGGGGAG ENSP00000370839.5:n.-39_-25delinsCAGTCGGGCGGGGAG
NM_000232.4:c.-39_-25delinsCAGTCGGGCGGGGAG , LRG_204t1:c.-39_-25delinsCAGTCGGGCGGGGAG NP_000223.1:n.-39_-25delinsCAGTCGGGCGGGGAG
XM_011534403.1:c.-39_-25delinsCAGTCGGGCGGGGAG XP_011532705.1:n.-39_-25delinsCAGTCGGGCGGGGAG
NM_000232.5:c.-39_-25delinsCAGTCGGGCGGGGAG MANE Select NP_000223.1:n.-39_-25delinsCAGTCGGGCGGGGAG