Canonical Allele Identifier: CA543053916

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1412541814
• gnomAD v2: 3-50383192-C-G
• gnomAD v3: 3-50345761-C-G
• gnomAD v4: 3-50345761-C-G
• MyVariant Identifiers: chr3:g.50383192C>G (hg19) ; chr3:g.50345761C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345761C>G , CM000665.2:g.50345761C>G	GRCh38
NC_000003.11:g.50383192C>G , CM000665.1:g.50383192C>G	GRCh37
NC_000003.10:g.50358196C>G	NCBI36
NG_023270.1:g.176G>C
NG_042828.1:g.4986G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-182G>C	ENSP00000231749.3:n.-182G>C
XM_005265216.2:c.-310G>C	XP_005265273.1:n.-310G>C