Canonical Allele Identifier: CA796086507
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs535392972
gnomAD v4: 4-52038318-G-T
MyVariant Identifiers: chr4:g.52904484G>T (hg19) chr4:g.52038318G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038318G>T , CM000666.2:g.52038318G>T GRCh38
NC_000004.11:g.52904484G>T , CM000666.1:g.52904484G>T GRCh37
NC_000004.10:g.52599241G>T NCBI36
NG_008891.1:g.5002C>A , LRG_204:g.5002C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-59C>A ENSP00000370839.5:n.-59C>A
NM_000232.4:c.-59C>A , LRG_204t1:c.-59C>A NP_000223.1:n.-59C>A
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