Canonical Allele Identifier: CA247018962
Gene: SGCG HGNC NCBI

Linked Data

dbSNP Id: rs534376978
gnomAD v3: 13-23170145-A-T
gnomAD v4: 13-23170145-A-T
MyVariant Identifiers: chr13:g.23744284A>T (hg19) chr13:g.23170145A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23170145A>T , CM000675.2:g.23170145A>T GRCh38
NC_000013.10:g.23744284A>T , CM000675.1:g.23744284A>T GRCh37
NC_000013.9:g.22642284A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_006719861.2:c.54+9499A>T XP_006719924.1:n.54+9499A>T
XM_006719861.3:c.54+9499A>T XP_006719924.1:n.54+9499A>T
NM_001378244.1:c.54+9499A>T NP_001365173.1:n.54+9499A>T
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