Canonical Allele Identifier: CA1457429176
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028111A= , CM000666.2:g.52028111A= GRCh38
NC_000004.11:g.52894277A= , CM000666.1:g.52894277A= GRCh37
NC_000004.10:g.52589034A= NCBI36
NG_008891.1:g.15209T= , LRG_204:g.15209T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.622-12T= MANE Select ENSP00000370839.6:n.622-12T=
ENST00000381431.9:c.622-12T= ENSP00000370839.5:n.622-12T=
NM_000232.4:c.622-12T= , LRG_204t1:c.622-12T= NP_000223.1:n.622-12T=
XM_006714049.2:c.325-12T= XP_006714112.1:n.325-12T=
XM_011534403.1:c.412-12T= XP_011532705.1:n.412-12T=
XM_011534404.1:c.325-12T= XP_011532706.1:n.325-12T=
NM_000232.5:c.622-12T= MANE Select NP_000223.1:n.622-12T=