Canonical Allele Identifier: CA1457434197
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038259T= , CM000666.2:g.52038259T= GRCh38
NC_000004.11:g.52904425T= , CM000666.1:g.52904425T= GRCh37
NC_000004.10:g.52599182T= NCBI36
NG_008891.1:g.5061A= , LRG_204:g.5061A=

Transcript Alleles

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