Canonical Allele Identifier: CA507756821

Gene: ZNF224

Linked Data

• dbSNP Id: rs4459653
• MyVariant Identifiers: chr19:g.44599615C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44095462C>G , CM000681.2:g.44095462C>G	GRCh38
NC_000019.9:g.44599615C>G , CM000681.1:g.44599615C>G	GRCh37
NC_000019.8:g.49291455C>G	NCBI36
NG_051221.1:g.6134C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684943.1:c.-69+932C>G	ENSP00000509045.1:n.-69+932C>G
ENST00000693561.1:c.-157-881C>G MANE Select	ENSP00000508532.1:n.-157-881C>G
ENST00000336976.10:c.-157-881C>G	ENSP00000337368.5:n.-157-881C>G
ENST00000586978.1:n.374+304C>G
ENST00000589060.1:n.1073C>G
ENST00000589680.5:c.-157-881C>G	ENSP00000465000.1:n.-157-881C>G
ENST00000590614.5:n.103-881C>G
NM_013398.2:c.-157-881C>G	NP_037530.2:n.-157-881C>G
XM_005259221.2:c.-157-881C>G	XP_005259278.1:n.-157-881C>G
NM_001321645.1:c.-157-881C>G	NP_001308574.1:n.-157-881C>G
NM_013398.3:c.-157-881C>G	NP_037530.2:n.-157-881C>G
XM_017027261.2:c.-1038C>G	XP_016882750.1:n.-1038C>G
NM_001321645.2:c.-157-881C>G	NP_001308574.1:n.-157-881C>G
NM_013398.4:c.-157-881C>G	NP_037530.2:n.-157-881C>G
NM_001321645.3:c.-157-881C>G MANE Select	NP_001308574.1:n.-157-881C>G
NM_013398.5:c.-157-881C>G	NP_037530.2:n.-157-881C>G