Canonical Allele Identifier: CA1457429142
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028027C= , CM000666.2:g.52028027C= GRCh38
NC_000004.11:g.52894193C= , CM000666.1:g.52894193C= GRCh37
NC_000004.10:g.52588950C= NCBI36
NG_008891.1:g.15293G= , LRG_204:g.15293G=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.694G= MANE Select ENSP00000370839.6:p.Val232=
ENST00000381431.9:c.694G= ENSP00000370839.5:p.Val232=
NM_000232.4:c.694G= , LRG_204t1:c.694G= NP_000223.1:p.Val232=
XM_006714049.2:c.397G= XP_006714112.1:p.Val133=
XM_011534403.1:c.484G= XP_011532705.1:p.Val162=
XM_011534404.1:c.397G= XP_011532706.1:p.Val133=
NM_000232.5:c.694G= MANE Select NP_000223.1:p.Val232=