Canonical Allele Identifier: CA247018965
Gene: SGCG HGNC NCBI

Linked Data

dbSNP Id: rs948851366
MyVariant Identifiers: chr13:g.23744321A>G (hg19) chr13:g.23170182A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23170182A>G , CM000675.2:g.23170182A>G GRCh38
NC_000013.10:g.23744321A>G , CM000675.1:g.23744321A>G GRCh37
NC_000013.9:g.22642321A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_006719861.2:c.54+9536A>G XP_006719924.1:n.54+9536A>G
XM_006719861.3:c.54+9536A>G XP_006719924.1:n.54+9536A>G
NM_001378244.1:c.54+9536A>G NP_001365173.1:n.54+9536A>G
Search 100 bp 5'
Search 100 bp 3'