Canonical Allele Identifier: CA2670614951
Gene: SGCB HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-204A>G ENSP00000370839.5:n.-204A>G
Search 100 bp 5'
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