Canonical Allele Identifier: CA1457429162
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028080C= , CM000666.2:g.52028080C= GRCh38
NC_000004.11:g.52894246C= , CM000666.1:g.52894246C= GRCh37
NC_000004.10:g.52589003C= NCBI36
NG_008891.1:g.15240G= , LRG_204:g.15240G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.641G= MANE Select ENSP00000370839.6:p.Ser214=
ENST00000381431.9:c.641G= ENSP00000370839.5:p.Ser214=
NM_000232.4:c.641G= , LRG_204t1:c.641G= NP_000223.1:p.Ser214=
XM_006714049.2:c.344G= XP_006714112.1:p.Ser115=
XM_011534403.1:c.431G= XP_011532705.1:p.Ser144=
XM_011534404.1:c.344G= XP_011532706.1:p.Ser115=
NM_000232.5:c.641G= MANE Select NP_000223.1:p.Ser214=