Canonical Allele Identifier: CA2670614732
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038308-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038308C>T , CM000666.2:g.52038308C>T GRCh38
NC_000004.11:g.52904474C>T , CM000666.1:g.52904474C>T GRCh37
NC_000004.10:g.52599231C>T NCBI36
NG_008891.1:g.5012G>A , LRG_204:g.5012G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-49G>A ENSP00000370839.5:n.-49G>A
NM_000232.4:c.-49G>A , LRG_204t1:c.-49G>A NP_000223.1:n.-49G>A
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