Canonical Allele Identifier: CA1457429088
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027910A= , CM000666.2:g.52027910A= GRCh38
NC_000004.11:g.52894076A= , CM000666.1:g.52894076A= GRCh37
NC_000004.10:g.52588833A= NCBI36
NG_008891.1:g.15410T= , LRG_204:g.15410T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+58T= MANE Select ENSP00000370839.6:n.753+58T=
ENST00000381431.9:c.753+58T= ENSP00000370839.5:n.753+58T=
NM_000232.4:c.753+58T= , LRG_204t1:c.753+58T= NP_000223.1:n.753+58T=
XM_006714049.2:c.456+58T= XP_006714112.1:n.456+58T=
XM_011534403.1:c.543+58T= XP_011532705.1:n.543+58T=
XM_011534404.1:c.456+58T= XP_011532706.1:n.456+58T=
NM_000232.5:c.753+58T= MANE Select NP_000223.1:n.753+58T=