Canonical Allele Identifier: CA580675385

Gene: ESCO2

Linked Data

• dbSNP Id: rs1196374413
• gnomAD v2: 8-27637788-A-G
• gnomAD v4: 8-27780271-A-G
• MyVariant Identifiers: chr8:g.27637788A>G (hg19) ; chr8:g.27780271A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27780271A>G , CM000670.2:g.27780271A>G	GRCh38
NC_000008.10:g.27637788A>G , CM000670.1:g.27637788A>G	GRCh37
NC_000008.9:g.27693707A>G	NCBI36
NG_008117.1:g.10731A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305188.13:c.955+4A>G MANE Select	ENSP00000306999.8:n.955+4A>G
ENST00000305188.12:c.955+4A>G	ENSP00000306999.8:n.955+4A>G
ENST00000518262.5:c.69+4A>G
ENST00000522378.5:c.861+3102A>G	ENSP00000428928.1:n.861+3102A>G
NM_001017420.2:c.955+4A>G	NP_001017420.1:n.955+4A>G
XM_011544421.1:c.955+4A>G	XP_011542723.1:n.955+4A>G
XM_011544422.1:c.955+4A>G	XP_011542724.1:n.955+4A>G
XR_949378.1:n.1039+4A>G
XR_949379.1:n.1039+4A>G
XM_011544421.2:c.955+4A>G	XP_011542723.1:n.955+4A>G
XM_011544422.2:c.955+4A>G	XP_011542724.1:n.955+4A>G
XR_949378.3:n.1039+4A>G
NM_001017420.3:c.955+4A>G MANE Select	NP_001017420.1:n.955+4A>G