Canonical Allele Identifier: CA1457434133
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038173A= , CM000666.2:g.52038173A= GRCh38
NC_000004.11:g.52904339A= , CM000666.1:g.52904339A= GRCh37
NC_000004.10:g.52599096A= NCBI36
NG_008891.1:g.5147T= , LRG_204:g.5147T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.33+54T= MANE Select ENSP00000370839.6:n.33+54T=
ENST00000381431.9:c.33+54T= ENSP00000370839.5:n.33+54T=
ENST00000506357.5:c.19+54T=
NM_000232.4:c.33+54T= , LRG_204t1:c.33+54T= NP_000223.1:n.33+54T=
XM_011534403.1:c.33+54T= XP_011532705.1:n.33+54T=
NM_000232.5:c.33+54T= MANE Select NP_000223.1:n.33+54T=