Canonical Allele Identifier: CA1765924723
Community Standard Title: NM_139167.4(SGCZ):c.40-104859A=
Gene: SGCZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.14659785T= , CM000670.2:g.14659785T= GRCh38
NC_000008.10:g.14517294T= , CM000670.1:g.14517294T= GRCh37
NC_000008.9:g.14561665T= NCBI36
NG_008899.1:g.583499A= , LRG_208:g.583499A=

Transcript Alleles

HGVS Amino-acid Change
NM_139167.4:c.40-104859A= MANE Select NP_631906.2:n.40-104859A=
ENST00000382080.6:c.40-104859A= MANE Select ENSP00000371512.1:n.40-104859A=
NM_001322879.1:c.40-104859A= NP_001309808.1:n.40-104859A=
NM_001322879.2:c.40-104859A= NP_001309808.1:n.40-104859A=
NM_001322880.1:c.40-104859A= NP_001309809.1:n.40-104859A=
NM_001322880.2:c.40-104859A= NP_001309809.1:n.40-104859A=
NM_001322881.1:c.-89-104859A= NP_001309810.1:n.-89-104859A=
NM_001322881.2:c.-89-104859A= NP_001309810.1:n.-89-104859A=
NM_139167.2:c.40-104859A= , LRG_208t1:c.40-104859A= NP_631906.2:n.40-104859A=
NM_139167.3:c.40-104859A= NP_631906.2:n.40-104859A=
ENST00000382080.5:c.40-104859A= ENSP00000371512.1:n.40-104859A=