Canonical Allele Identifier: CA1457430026
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52029854C= , CM000666.2:g.52029854C= GRCh38
NC_000004.11:g.52896020C= , CM000666.1:g.52896020C= GRCh37
NC_000004.10:g.52590777C= NCBI36
NG_008891.1:g.13466G= , LRG_204:g.13466G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.253G= MANE Select ENSP00000370839.6:p.Val85=
ENST00000381431.9:c.253G= ENSP00000370839.5:p.Val85=
ENST00000506357.5:c.336G=
ENST00000514133.1:c.330G= ENSP00000425818.1:n.330G=
NM_000232.4:c.253G= , LRG_204t1:c.253G= NP_000223.1:p.Val85=
XM_006714049.2:c.-45G= XP_006714112.1:n.-45G=
XM_011534403.1:c.43G= XP_011532705.1:p.Val15=
XM_011534404.1:c.-45G= XP_011532706.1:n.-45G=
NM_000232.5:c.253G= MANE Select NP_000223.1:p.Val85=