Canonical Allele Identifier: CA2576089595
Gene: ZNF469 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88427451A>G , CM000678.2:g.88427451A>G GRCh38
NC_000016.9:g.88493859A>G , CM000678.1:g.88493859A>G GRCh37
NC_000016.8:g.87021360A>G NCBI36
NG_012236.2:g.4981A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000565624.3:c.-20A>G MANE Select ENSP00000456500.2:n.-20A>G
XM_011523386.1:c.-20A>G XP_011521688.1:n.-20A>G
XM_011523387.1:c.-20A>G XP_011521689.1:n.-20A>G
XM_011523388.1:c.-20A>G XP_011521690.1:n.-20A>G
XM_017023784.1:c.-20A>G XP_016879273.1:n.-20A>G
XM_017023785.1:c.-20A>G XP_016879274.1:n.-20A>G
XR_002957934.1:n.250+2513T>C
NM_001367624.2:c.-20A>G MANE Select NP_001354553.1:n.-20A>G
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