Canonical Allele Identifier: CA1457429065
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027865_52027867delinsAAT , CM000666.2:g.52027865_52027867delinsAAT GRCh38
NC_000004.11:g.52894031_52894033delinsAAT , CM000666.1:g.52894031_52894033delinsAAT GRCh37
NC_000004.10:g.52588788_52588790delinsAAT NCBI36
NG_008891.1:g.15453_15455delinsATT , LRG_204:g.15453_15455delinsATT

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+101_753+103delinsATT MANE Select ENSP00000370839.6:n.753+101_753+103delins...
ENST00000381431.9:c.753+101_753+103delinsATT ENSP00000370839.5:n.753+101_753+103delins...
NM_000232.4:c.753+101_753+103delinsATT , LRG_204t1:c.753+101_753+103delinsATT NP_000223.1:n.753+101_753+103delinsATT
XM_006714049.2:c.456+101_456+103delinsATT XP_006714112.1:n.456+101_456+103delinsATT...
XM_011534403.1:c.543+101_543+103delinsATT XP_011532705.1:n.543+101_543+103delinsATT...
XM_011534404.1:c.456+101_456+103delinsATT XP_011532706.1:n.456+101_456+103delinsATT...
NM_000232.5:c.753+101_753+103delinsATT MANE Select NP_000223.1:n.753+101_753+103delinsATT