Canonical Allele Identifier: CA1457434196
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038258A= , CM000666.2:g.52038258A= GRCh38
NC_000004.11:g.52904424A= , CM000666.1:g.52904424A= GRCh37
NC_000004.10:g.52599181A= NCBI36
NG_008891.1:g.5062T= , LRG_204:g.5062T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.2T= MANE Select ENSP00000370839.6:p.Met1=
ENST00000381431.9:c.2T= ENSP00000370839.5:p.Met1=
NM_000232.4:c.2T= , LRG_204t1:c.2T= NP_000223.1:p.Met1=
XM_011534403.1:c.2T= XP_011532705.1:p.Met1=
NM_000232.5:c.2T= MANE Select NP_000223.1:p.Met1=