Canonical Allele Identifier: CA2578086694
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033387A>G , CM000666.2:g.52033387A>G GRCh38
NC_000004.11:g.52899553A>G , CM000666.1:g.52899553A>G GRCh37
NC_000004.10:g.52594310A>G NCBI36
NG_008891.1:g.9933T>C , LRG_204:g.9933T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.243+44T>C MANE Select ENSP00000370839.6:n.243+44T>C
ENST00000381431.9:c.243+44T>C ENSP00000370839.5:n.243+44T>C
ENST00000506357.5:c.229+44T>C
ENST00000514133.1:c.210+44T>C ENSP00000425818.1:n.210+44T>C
NM_000232.4:c.243+44T>C , LRG_204t1:c.243+44T>C NP_000223.1:n.243+44T>C
XM_006714049.2:c.-165+44T>C XP_006714112.1:n.-165+44T>C
XM_011534403.1:c.34-3524T>C XP_011532705.1:n.34-3524T>C
XM_011534404.1:c.-142+44T>C XP_011532706.1:n.-142+44T>C
NM_000232.5:c.243+44T>C MANE Select NP_000223.1:n.243+44T>C