Canonical Allele Identifier: CA1457429119
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027981A= , CM000666.2:g.52027981A= GRCh38
NC_000004.11:g.52894147A= , CM000666.1:g.52894147A= GRCh37
NC_000004.10:g.52588904A= NCBI36
NG_008891.1:g.15339T= , LRG_204:g.15339T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.740T= MANE Select ENSP00000370839.6:p.Met247=
ENST00000381431.9:c.740T= ENSP00000370839.5:p.Met247=
NM_000232.4:c.740T= , LRG_204t1:c.740T= NP_000223.1:p.Met247=
XM_006714049.2:c.443T= XP_006714112.1:p.Met148=
XM_011534403.1:c.530T= XP_011532705.1:p.Met177=
XM_011534404.1:c.443T= XP_011532706.1:p.Met148=
NM_000232.5:c.740T= MANE Select NP_000223.1:p.Met247=