Canonical Allele Identifier: CA172689491
Gene: SGCZ HGNC NCBI

Linked Data

dbSNP Id: rs11989868
MyVariant Identifiers: chr8:g.14692647A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.14692647A>T , CM000670.2:g.14692647A>T GRCh38
NC_000008.10:g.14550156A>T , CM000670.1:g.14550156A>T GRCh37
NC_000008.9:g.14594527A>T NCBI36
NG_008899.1:g.550637T>A , LRG_208:g.550637T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382080.6:c.40-137721T>A MANE Select ENSP00000371512.1:n.40-137721T>A
ENST00000382080.5:c.40-137721T>A ENSP00000371512.1:n.40-137721T>A
NM_139167.2:c.40-137721T>A , LRG_208t1:c.40-137721T>A NP_631906.2:n.40-137721T>A
NM_001322879.1:c.40-137721T>A NP_001309808.1:n.40-137721T>A
NM_001322880.1:c.40-137721T>A NP_001309809.1:n.40-137721T>A
NM_001322881.1:c.-89-137721T>A NP_001309810.1:n.-89-137721T>A
NM_139167.3:c.40-137721T>A NP_631906.2:n.40-137721T>A
NM_139167.4:c.40-137721T>A MANE Select NP_631906.2:n.40-137721T>A
NM_001322879.2:c.40-137721T>A NP_001309808.1:n.40-137721T>A
NM_001322880.2:c.40-137721T>A NP_001309809.1:n.40-137721T>A
NM_001322881.2:c.-89-137721T>A NP_001309810.1:n.-89-137721T>A