Canonical Allele Identifier: CA1457429060
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027860_52027861delinsCA , CM000666.2:g.52027860_52027861delinsCA GRCh38
NC_000004.11:g.52894026_52894027delinsCA , CM000666.1:g.52894026_52894027delinsCA GRCh37
NC_000004.10:g.52588783_52588784delinsCA NCBI36
NG_008891.1:g.15459_15460delinsTG , LRG_204:g.15459_15460delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+107_753+108delinsTG MANE Select ENSP00000370839.6:n.753+107_753+108delins...
ENST00000381431.9:c.753+107_753+108delinsTG ENSP00000370839.5:n.753+107_753+108delins...
NM_000232.4:c.753+107_753+108delinsTG , LRG_204t1:c.753+107_753+108delinsTG NP_000223.1:n.753+107_753+108delinsTG
XM_006714049.2:c.456+107_456+108delinsTG XP_006714112.1:n.456+107_456+108delinsTG
XM_011534403.1:c.543+107_543+108delinsTG XP_011532705.1:n.543+107_543+108delinsTG
XM_011534404.1:c.456+107_456+108delinsTG XP_011532706.1:n.456+107_456+108delinsTG
NM_000232.5:c.753+107_753+108delinsTG MANE Select NP_000223.1:n.753+107_753+108delinsTG