Canonical Allele Identifier: CA96791874
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1005789246
gnomAD v3: 4-52038396-A-T
gnomAD v4: 4-52038396-A-T
MyVariant Identifiers: chr4:g.52904562A>T (hg19) chr4:g.52038396A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038396A>T , CM000666.2:g.52038396A>T GRCh38
NC_000004.11:g.52904562A>T , CM000666.1:g.52904562A>T GRCh37
NC_000004.10:g.52599319A>T NCBI36
NG_008891.1:g.4924T>A , LRG_204:g.4924T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-137T>A ENSP00000370839.5:n.-137T>A
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