Canonical Allele Identifier: CA184463882

Gene: ZHX2

Linked Data

• dbSNP Id: rs1005886385
• gnomAD v3: 8-122960934-T-G
• gnomAD v4: 8-122960934-T-G
• MyVariant Identifiers: chr8:g.123973174T>G (hg19) ; chr8:g.122960934T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122960934T>G , CM000670.2:g.122960934T>G	GRCh38
NC_000008.10:g.123973174T>G , CM000670.1:g.123973174T>G	GRCh37
NC_000008.9:g.124042355T>G	NCBI36
NG_046951.1:g.184586T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314393.6:c.*4+6906T>G MANE Select	ENSP00000314709.4:n.*4+6906T>G
ENST00000314393.5:c.*4+6906T>G	ENSP00000314709.4:n.*4+6906T>G
NM_014943.3:c.*4+6906T>G	NP_055758.1:n.*4+6906T>G
XM_005250836.3:c.*4+6906T>G	XP_005250893.1:n.*4+6906T>G
XM_005250837.3:c.*4+6906T>G	XP_005250894.1:n.*4+6906T>G
XM_011516931.1:c.*4+6906T>G	XP_011515233.1:n.*4+6906T>G
XM_011516932.1:c.*4+6906T>G	XP_011515234.1:n.*4+6906T>G
NM_001362797.1:c.*4+6906T>G	NP_001349726.1:n.*4+6906T>G
NM_014943.4:c.*4+6906T>G	NP_055758.1:n.*4+6906T>G
XM_005250836.5:c.*4+6906T>G	XP_005250893.1:n.*4+6906T>G
XM_011516932.3:c.*4+6906T>G	XP_011515234.1:n.*4+6906T>G
NM_014943.5:c.*4+6906T>G MANE Select	NP_055758.1:n.*4+6906T>G
NM_001362797.2:c.*4+6906T>G	NP_001349726.1:n.*4+6906T>G