Canonical Allele Identifier: CA2670614745
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038315-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038315A>T , CM000666.2:g.52038315A>T GRCh38
NC_000004.11:g.52904481A>T , CM000666.1:g.52904481A>T GRCh37
NC_000004.10:g.52599238A>T NCBI36
NG_008891.1:g.5005T>A , LRG_204:g.5005T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-56T>A ENSP00000370839.5:n.-56T>A
NM_000232.4:c.-56T>A , LRG_204t1:c.-56T>A NP_000223.1:n.-56T>A
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