Canonical Allele Identifier: CA1766199743
Gene: SGCZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.15069658T= , CM000670.2:g.15069658T= GRCh38
NC_000008.10:g.14927167T= , CM000670.1:g.14927167T= GRCh37
NC_000008.9:g.14971538T= NCBI36
NG_008899.1:g.173626A= , LRG_208:g.173626A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382080.6:c.39+167927A= MANE Select ENSP00000371512.1:n.39+167927A=
ENST00000382080.5:c.39+167927A= ENSP00000371512.1:n.39+167927A=
NM_139167.2:c.39+167927A= , LRG_208t1:c.39+167927A= NP_631906.2:n.39+167927A=
NM_001322879.1:c.39+167927A= NP_001309808.1:n.39+167927A=
NM_001322880.1:c.39+167927A= NP_001309809.1:n.39+167927A=
NM_001322881.1:c.-90+167927A= NP_001309810.1:n.-90+167927A=
NM_139167.3:c.39+167927A= NP_631906.2:n.39+167927A=
NM_139167.4:c.39+167927A= MANE Select NP_631906.2:n.39+167927A=
NM_001322879.2:c.39+167927A= NP_001309808.1:n.39+167927A=
NM_001322880.2:c.39+167927A= NP_001309809.1:n.39+167927A=
NM_001322881.2:c.-90+167927A= NP_001309810.1:n.-90+167927A=