Canonical Allele Identifier: CA286371163
Gene: ZNF469 HGNC NCBI

Linked Data

dbSNP Id: rs930397228
MyVariant Identifiers: chr16:g.88493875G>C (hg19) chr16:g.88427467G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88427467G>C , CM000678.2:g.88427467G>C GRCh38
NC_000016.9:g.88493875G>C , CM000678.1:g.88493875G>C GRCh37
NC_000016.8:g.87021376G>C NCBI36
NG_012236.2:g.4997G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000565624.3:c.-4G>C MANE Select ENSP00000456500.2:n.-4G>C
XM_011523386.1:c.-4G>C XP_011521688.1:n.-4G>C
XM_011523387.1:c.-4G>C XP_011521689.1:n.-4G>C
XM_011523388.1:c.-4G>C XP_011521690.1:n.-4G>C
XM_017023784.1:c.-4G>C XP_016879273.1:n.-4G>C
XM_017023785.1:c.-4G>C XP_016879274.1:n.-4G>C
XR_002957934.1:n.250+2497C>G
NM_001367624.2:c.-4G>C MANE Select NP_001354553.1:n.-4G>C
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