Canonical Allele Identifier: CA1766199705

Gene: SGCZ

Linked Data

• dbSNP Id: rs1805278309

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.15069613T>C , CM000670.2:g.15069613T>C	GRCh38
NC_000008.10:g.14927122T>C , CM000670.1:g.14927122T>C	GRCh37
NC_000008.9:g.14971493T>C	NCBI36
NG_008899.1:g.173671A>G , LRG_208:g.173671A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382080.6:c.39+167972A>G MANE Select	ENSP00000371512.1:n.39+167972A>G
ENST00000382080.5:c.39+167972A>G	ENSP00000371512.1:n.39+167972A>G
NM_139167.2:c.39+167972A>G , LRG_208t1:c.39+167972A>G	NP_631906.2:n.39+167972A>G
NM_001322879.1:c.39+167972A>G	NP_001309808.1:n.39+167972A>G
NM_001322880.1:c.39+167972A>G	NP_001309809.1:n.39+167972A>G
NM_001322881.1:c.-90+167972A>G	NP_001309810.1:n.-90+167972A>G
NM_139167.3:c.39+167972A>G	NP_631906.2:n.39+167972A>G
NM_139167.4:c.39+167972A>G MANE Select	NP_631906.2:n.39+167972A>G
NM_001322879.2:c.39+167972A>G	NP_001309808.1:n.39+167972A>G
NM_001322880.2:c.39+167972A>G	NP_001309809.1:n.39+167972A>G
NM_001322881.2:c.-90+167972A>G	NP_001309810.1:n.-90+167972A>G