Canonical Allele Identifier: CA551344208
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1412066114
gnomAD v2: 4-52904492-CGCGCCT-C
gnomAD v3: 4-52038326-CGCGCCT-C
gnomAD v4: 4-52038326-CGCGCCT-C
MyVariant Identifiers: chr4:g.52904493_52904498del (hg19) chr4:g.52038327_52038332del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038331_52038336del , CM000666.2:g.52038331_52038336del GRCh38
NC_000004.11:g.52904497_52904502del , CM000666.1:g.52904497_52904502del GRCh37
NC_000004.10:g.52599254_52599259del NCBI36
NG_008891.1:g.4988_4993del , LRG_204:g.4988_4993del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-73_-68del ENSP00000370839.5:n.-73_-68del
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