Canonical Allele Identifier: CA96791985
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs898869131
gnomAD v2: 4-52904638-GC-G
gnomAD v3: 4-52038472-GC-G
gnomAD v4: 4-52038472-GC-G
MyVariant Identifiers: chr4:g.52904639del (hg19) chr4:g.52038473del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038473del , CM000666.2:g.52038473del GRCh38
NC_000004.11:g.52904639del , CM000666.1:g.52904639del GRCh37
NC_000004.10:g.52599396del NCBI36
NG_008891.1:g.4847del , LRG_204:g.4847del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-214del ENSP00000370839.5:n.-214del
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