Canonical Allele Identifier: CA96791861
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs942697032
gnomAD v3: 4-52038377-C-T
gnomAD v4: 4-52038377-C-T
MyVariant Identifiers: chr4:g.52904543C>T (hg19) chr4:g.52038377C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038377C>T , CM000666.2:g.52038377C>T GRCh38
NC_000004.11:g.52904543C>T , CM000666.1:g.52904543C>T GRCh37
NC_000004.10:g.52599300C>T NCBI36
NG_008891.1:g.4943G>A , LRG_204:g.4943G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-118G>A ENSP00000370839.5:n.-118G>A
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