Canonical Allele Identifier: CA1457429150
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028047A= , CM000666.2:g.52028047A= GRCh38
NC_000004.11:g.52894213A= , CM000666.1:g.52894213A= GRCh37
NC_000004.10:g.52588970A= NCBI36
NG_008891.1:g.15273T= , LRG_204:g.15273T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.674T= MANE Select ENSP00000370839.6:p.Ile225=
ENST00000381431.9:c.674T= ENSP00000370839.5:p.Ile225=
NM_000232.4:c.674T= , LRG_204t1:c.674T= NP_000223.1:p.Ile225=
XM_006714049.2:c.377T= XP_006714112.1:p.Ile126=
XM_011534403.1:c.464T= XP_011532705.1:p.Ile155=
XM_011534404.1:c.377T= XP_011532706.1:p.Ile126=
NM_000232.5:c.674T= MANE Select NP_000223.1:p.Ile225=