Canonical Allele Identifier: CA214439
Gene: ZMYND10 HGNC NCBI

Linked Data

ClinVar Variation Id: 66021
dbSNP Id: rs138815960
gnomAD v2: 3-50382964-A-C
gnomAD v3: 3-50345533-A-C
gnomAD v4: 3-50345533-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345533A>C , CM000665.2:g.50345533A>C GRCh38
NC_000003.11:g.50382964A>C , CM000665.1:g.50382964A>C GRCh37
NC_000003.10:g.50357968A>C NCBI36
NG_023270.1:g.404T>G
NG_042828.1:g.5214T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000231749.8:c.47T>G MANE Select ENSP00000231749.3:p.Val16Gly
ENST00000231749.7:c.47T>G ENSP00000231749.3:p.Val16Gly
ENST00000360165.7:c.47T>G ENSP00000353289.3:p.Val16Gly
ENST00000431869.1:c.47T>G ENSP00000391545.1:p.Val16Gly
ENST00000442887.1:c.-38+2T>G ENSP00000393687.1:n.-38+2T>G
ENST00000443080.5:c.47T>G ENSP00000415661.1:p.Val16Gly
ENST00000468182.1:n.149T>G
NM_001308379.1:c.47T>G NP_001295308.1:p.Val16Gly
NM_015896.2:c.47T>G NP_056980.2:p.Val16Gly
NM_015896.3:c.47T>G NP_056980.2:p.Val16Gly
XM_005265216.2:c.-82T>G XP_005265273.1:n.-82T>G
XM_005265216.3:c.-82T>G XP_005265273.1:n.-82T>G
NM_015896.4:c.47T>G MANE Select NP_056980.2:p.Val16Gly
NM_001308379.2:c.47T>G NP_001295308.1:p.Val16Gly