Canonical Allele Identifier: CA387502531
Gene: SGCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23203791A>G , CM000675.2:g.23203791A>G GRCh38
NC_000013.10:g.23777930A>G , CM000675.1:g.23777930A>G GRCh37
NC_000013.9:g.22675930A>G NCBI36
NG_008759.1:g.27871A>G , LRG_207:g.27871A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218867.4:c.97A>G MANE Select ENSP00000218867.3:p.Lys33Glu
ENST00000218867.3:c.97A>G ENSP00000218867.3:p.Lys33Glu
NM_000231.2:c.97A>G , LRG_207t1:c.97A>G NP_000222.1:p.Lys33Glu
XM_005266505.2:c.97A>G XP_005266562.1:p.Lys33Glu
XM_006719861.2:c.151A>G XP_006719924.1:p.Lys51Glu
XM_006719861.3:c.151A>G XP_006719924.1:p.Lys51Glu
XM_024449397.1:c.97A>G XP_024305165.1:p.Lys33Glu
NM_000231.3:c.97A>G MANE Select NP_000222.2:p.Lys33Glu
NM_001378244.1:c.151A>G NP_001365173.1:p.Lys51Glu
NM_001378245.1:c.97A>G NP_001365174.1:p.Lys33Glu
NM_001378246.1:c.97A>G NP_001365175.1:p.Lys33Glu