Canonical Allele Identifier: CA2670614741
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038312-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038312G>T , CM000666.2:g.52038312G>T GRCh38
NC_000004.11:g.52904478G>T , CM000666.1:g.52904478G>T GRCh37
NC_000004.10:g.52599235G>T NCBI36
NG_008891.1:g.5008C>A , LRG_204:g.5008C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-53C>A ENSP00000370839.5:n.-53C>A
NM_000232.4:c.-53C>A , LRG_204t1:c.-53C>A NP_000223.1:n.-53C>A
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