Canonical Allele Identifier: CA397124556

Gene: ZNF469

Linked Data

• dbSNP Id: rs1906646528
• MyVariant Identifiers: chr16:g.88503592C>G (hg19) ; chr16:g.88437184C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88437184C>G , CM000678.2:g.88437184C>G	GRCh38
NC_000016.9:g.88503592C>G , CM000678.1:g.88503592C>G	GRCh37
NC_000016.8:g.87031093C>G	NCBI36
NG_012236.2:g.14714C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.9714C>G MANE Select	ENSP00000456500.2:p.His3238Gln
ENST00000437464.1:c.9630C>G	ENSP00000402343.1:p.His3210Gln
ENST00000565624.1:c.9714C>G	ENSP00000456500.1:p.His3238Gln
NM_001127464.2:c.9630C>G	NP_001120936.2:p.His3210Gln
XM_011523386.1:c.9714C>G	XP_011521688.1:p.His3238Gln
XM_011523387.1:c.9714C>G	XP_011521689.1:p.His3238Gln
XM_011523388.1:c.9714C>G	XP_011521690.1:p.His3238Gln
XM_017023784.1:c.9714C>G	XP_016879273.1:p.His3238Gln
XM_017023785.1:c.9714C>G	XP_016879274.1:p.His3238Gln
NM_001367624.1:c.9714C>G	NP_001354553.1:p.His3238Gln
NM_001367624.2:c.9714C>G MANE Select	NP_001354553.1:p.His3238Gln