Canonical Allele Identifier: CA796086699
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1252791679
gnomAD v3: 4-52038432-G-C
gnomAD v4: 4-52038432-G-C
MyVariant Identifiers: chr4:g.52904598G>C (hg19) chr4:g.52038432G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038432G>C , CM000666.2:g.52038432G>C GRCh38
NC_000004.11:g.52904598G>C , CM000666.1:g.52904598G>C GRCh37
NC_000004.10:g.52599355G>C NCBI36
NG_008891.1:g.4888C>G , LRG_204:g.4888C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-173C>G ENSP00000370839.5:n.-173C>G
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