Canonical Allele Identifier: CA907889699

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1480238204
• gnomAD v3: 3-50342739-A-G
• gnomAD v4: 3-50342739-A-G
• MyVariant Identifiers: chr3:g.50380170A>G (hg19) ; chr3:g.50342739A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342739A>G , CM000665.2:g.50342739A>G	GRCh38
NC_000003.11:g.50380170A>G , CM000665.1:g.50380170A>G	GRCh37
NC_000003.10:g.50355174A>G	NCBI36
NG_023270.1:g.3198T>C
NG_042828.1:g.8008T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.701-170T>C MANE Select	ENSP00000231749.3:n.701-170T>C
ENST00000231749.7:c.701-170T>C	ENSP00000231749.3:n.701-170T>C
ENST00000360165.7:c.600-84T>C	ENSP00000353289.3:n.600-84T>C
ENST00000442887.1:c.572-170T>C	ENSP00000393687.1:n.572-170T>C
ENST00000443080.5:c.*453-170T>C	ENSP00000415661.1:n.*453-170T>C
ENST00000475688.1:n.430T>C
NM_001308379.1:c.600-84T>C	NP_001295308.1:n.600-84T>C
NM_015896.2:c.701-170T>C	NP_056980.2:n.701-170T>C
NM_015896.3:c.701-170T>C	NP_056980.2:n.701-170T>C
XM_005265216.2:c.464-170T>C	XP_005265273.1:n.464-170T>C
XM_005265216.3:c.464-170T>C	XP_005265273.1:n.464-170T>C
NM_015896.4:c.701-170T>C MANE Select	NP_056980.2:n.701-170T>C
NM_001308379.2:c.600-84T>C	NP_001295308.1:n.600-84T>C