Canonical Allele Identifier: CA1766199793

Gene: SGCZ

Linked Data

• dbSNP Id: rs1369442672

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.15069731T>G , CM000670.2:g.15069731T>G	GRCh38
NC_000008.10:g.14927240T>G , CM000670.1:g.14927240T>G	GRCh37
NC_000008.9:g.14971611T>G	NCBI36
NG_008899.1:g.173553A>C , LRG_208:g.173553A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382080.6:c.39+167854A>C MANE Select	ENSP00000371512.1:n.39+167854A>C
ENST00000382080.5:c.39+167854A>C	ENSP00000371512.1:n.39+167854A>C
NM_139167.2:c.39+167854A>C , LRG_208t1:c.39+167854A>C	NP_631906.2:n.39+167854A>C
NM_001322879.1:c.39+167854A>C	NP_001309808.1:n.39+167854A>C
NM_001322880.1:c.39+167854A>C	NP_001309809.1:n.39+167854A>C
NM_001322881.1:c.-90+167854A>C	NP_001309810.1:n.-90+167854A>C
NM_139167.3:c.39+167854A>C	NP_631906.2:n.39+167854A>C
NM_139167.4:c.39+167854A>C MANE Select	NP_631906.2:n.39+167854A>C
NM_001322879.2:c.39+167854A>C	NP_001309808.1:n.39+167854A>C
NM_001322880.2:c.39+167854A>C	NP_001309809.1:n.39+167854A>C
NM_001322881.2:c.-90+167854A>C	NP_001309810.1:n.-90+167854A>C