Canonical Allele Identifier: CA1457434181
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038237G= , CM000666.2:g.52038237G= GRCh38
NC_000004.11:g.52904403G= , CM000666.1:g.52904403G= GRCh37
NC_000004.10:g.52599160G= NCBI36
NG_008891.1:g.5083C= , LRG_204:g.5083C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.23C= MANE Select ENSP00000370839.6:p.Ala8=
ENST00000381431.9:c.23C= ENSP00000370839.5:p.Ala8=
ENST00000506357.5:c.9C=
NM_000232.4:c.23C= , LRG_204t1:c.23C= NP_000223.1:p.Ala8=
XM_011534403.1:c.23C= XP_011532705.1:p.Ala8=
NM_000232.5:c.23C= MANE Select NP_000223.1:p.Ala8=