Canonical Allele Identifier: CA1457429159
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028070_52028071delinsAT , CM000666.2:g.52028070_52028071delinsAT GRCh38
NC_000004.11:g.52894236_52894237delinsAT , CM000666.1:g.52894236_52894237delinsAT GRCh37
NC_000004.10:g.52588993_52588994delinsAT NCBI36
NG_008891.1:g.15249_15250delinsAT , LRG_204:g.15249_15250delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.650_651delinsAT MANE Select ENSP00000370839.6:p.Asn217=
ENST00000381431.9:c.650_651delinsAT ENSP00000370839.5:p.Asn217=
NM_000232.4:c.650_651delinsAT , LRG_204t1:c.650_651delinsAT NP_000223.1:p.Asn217=
XM_006714049.2:c.353_354delinsAT XP_006714112.1:p.Asn118=
XM_011534403.1:c.440_441delinsAT XP_011532705.1:p.Asn147=
XM_011534404.1:c.353_354delinsAT XP_011532706.1:p.Asn118=
NM_000232.5:c.650_651delinsAT MANE Select NP_000223.1:p.Asn217=