Canonical Allele Identifier: CA2078571259
Gene: SGCG HGNC NCBI

Linked Data

dbSNP Id: rs1876400150
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23170152G>C , CM000675.2:g.23170152G>C GRCh38
NC_000013.10:g.23744291G>C , CM000675.1:g.23744291G>C GRCh37
NC_000013.9:g.22642291G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_006719861.2:c.54+9506G>C XP_006719924.1:n.54+9506G>C
XM_006719861.3:c.54+9506G>C XP_006719924.1:n.54+9506G>C
NM_001378244.1:c.54+9506G>C NP_001365173.1:n.54+9506G>C
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