Canonical Allele Identifier: CA2670614952
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038463-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038463T>G , CM000666.2:g.52038463T>G GRCh38
NC_000004.11:g.52904629T>G , CM000666.1:g.52904629T>G GRCh37
NC_000004.10:g.52599386T>G NCBI36
NG_008891.1:g.4857A>C , LRG_204:g.4857A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-204A>C ENSP00000370839.5:n.-204A>C
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