Canonical Allele Identifier: CA172751984

Gene: SGCZ

Linked Data

• dbSNP Id: rs554245748
• gnomAD v3: 8-15069466-G-T
• gnomAD v4: 8-15069466-G-T
• MyVariant Identifiers: chr8:g.14926975G>T (hg19) ; chr8:g.15069466G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.15069466G>T , CM000670.2:g.15069466G>T	GRCh38
NC_000008.10:g.14926975G>T , CM000670.1:g.14926975G>T	GRCh37
NC_000008.9:g.14971346G>T	NCBI36
NG_008899.1:g.173818C>A , LRG_208:g.173818C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382080.6:c.39+168119C>A MANE Select	ENSP00000371512.1:n.39+168119C>A
ENST00000382080.5:c.39+168119C>A	ENSP00000371512.1:n.39+168119C>A
NM_139167.2:c.39+168119C>A , LRG_208t1:c.39+168119C>A	NP_631906.2:n.39+168119C>A
NM_001322879.1:c.39+168119C>A	NP_001309808.1:n.39+168119C>A
NM_001322880.1:c.39+168119C>A	NP_001309809.1:n.39+168119C>A
NM_001322881.1:c.-90+168119C>A	NP_001309810.1:n.-90+168119C>A
NM_139167.3:c.39+168119C>A	NP_631906.2:n.39+168119C>A
NM_139167.4:c.39+168119C>A MANE Select	NP_631906.2:n.39+168119C>A
NM_001322879.2:c.39+168119C>A	NP_001309808.1:n.39+168119C>A
NM_001322880.2:c.39+168119C>A	NP_001309809.1:n.39+168119C>A
NM_001322881.2:c.-90+168119C>A	NP_001309810.1:n.-90+168119C>A