Canonical Allele Identifier: CA1047834225

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1703428885
• gnomAD v3: 3-50342842-G-A
• gnomAD v4: 3-50342842-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342842G>A , CM000665.2:g.50342842G>A	GRCh38
NC_000003.11:g.50380273G>A , CM000665.1:g.50380273G>A	GRCh37
NC_000003.10:g.50355277G>A	NCBI36
NG_023270.1:g.3095C>T
NG_042828.1:g.7905C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+76C>T MANE Select	ENSP00000231749.3:n.700+76C>T
ENST00000231749.7:c.700+76C>T	ENSP00000231749.3:n.700+76C>T
ENST00000360165.7:c.600-187C>T	ENSP00000353289.3:n.600-187C>T
ENST00000442887.1:c.571+76C>T	ENSP00000393687.1:n.571+76C>T
ENST00000443080.5:c.*452+76C>T	ENSP00000415661.1:n.*452+76C>T
ENST00000475688.1:n.327C>T
NM_001308379.1:c.600-187C>T	NP_001295308.1:n.600-187C>T
NM_015896.2:c.700+76C>T	NP_056980.2:n.700+76C>T
NM_015896.3:c.700+76C>T	NP_056980.2:n.700+76C>T
XM_005265216.2:c.463+76C>T	XP_005265273.1:n.463+76C>T
XM_005265216.3:c.463+76C>T	XP_005265273.1:n.463+76C>T
NM_015896.4:c.700+76C>T MANE Select	NP_056980.2:n.700+76C>T
NM_001308379.2:c.600-187C>T	NP_001295308.1:n.600-187C>T