Canonical Allele Identifier: CA1457429067
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027866_52027867delinsAT , CM000666.2:g.52027866_52027867delinsAT GRCh38
NC_000004.11:g.52894032_52894033delinsAT , CM000666.1:g.52894032_52894033delinsAT GRCh37
NC_000004.10:g.52588789_52588790delinsAT NCBI36
NG_008891.1:g.15453_15454delinsAT , LRG_204:g.15453_15454delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+101_753+102delinsAT MANE Select ENSP00000370839.6:n.753+101_753+102delins...
ENST00000381431.9:c.753+101_753+102delinsAT ENSP00000370839.5:n.753+101_753+102delins...
NM_000232.4:c.753+101_753+102delinsAT , LRG_204t1:c.753+101_753+102delinsAT NP_000223.1:n.753+101_753+102delinsAT
XM_006714049.2:c.456+101_456+102delinsAT XP_006714112.1:n.456+101_456+102delinsAT
XM_011534403.1:c.543+101_543+102delinsAT XP_011532705.1:n.543+101_543+102delinsAT
XM_011534404.1:c.456+101_456+102delinsAT XP_011532706.1:n.456+101_456+102delinsAT
NM_000232.5:c.753+101_753+102delinsAT MANE Select NP_000223.1:n.753+101_753+102delinsAT