Canonical Allele Identifier: CA96791820
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs371352663
gnomAD v3: 4-52038348-C-A
gnomAD v4: 4-52038348-C-A
MyVariant Identifiers: chr4:g.52904514C>A (hg19) chr4:g.52038348C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038348C>A , CM000666.2:g.52038348C>A GRCh38
NC_000004.11:g.52904514C>A , CM000666.1:g.52904514C>A GRCh37
NC_000004.10:g.52599271C>A NCBI36
NG_008891.1:g.4972G>T , LRG_204:g.4972G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-89G>T ENSP00000370839.5:n.-89G>T
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