Canonical Allele Identifier: CA907891995

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1197112635
• gnomAD v3: 3-50345773-G-A
• gnomAD v4: 3-50345773-G-A
• MyVariant Identifiers: chr3:g.50383204G>A (hg19) ; chr3:g.50345773G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345773G>A , CM000665.2:g.50345773G>A	GRCh38
NC_000003.11:g.50383204G>A , CM000665.1:g.50383204G>A	GRCh37
NC_000003.10:g.50358208G>A	NCBI36
NG_023270.1:g.164C>T
NG_042828.1:g.4974C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-194C>T	ENSP00000231749.3:n.-194C>T
XM_005265216.2:c.-322C>T	XP_005265273.1:n.-322C>T