Canonical Allele Identifier: CA309817409
Gene: ZNF615 HGNC NCBI

Linked Data

dbSNP Id: rs1715
gnomAD v3: 19-51991525-T-C
gnomAD v4: 19-51991525-T-C
MyVariant Identifiers: chr19:g.52494778T>C (hg19) chr19:g.51991525T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51991525T>C , CM000681.2:g.51991525T>C GRCh38
NC_000019.9:g.52494778T>C , CM000681.1:g.52494778T>C GRCh37
NC_000019.8:g.57186590T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000598071.6:c.*1355A>G MANE Select ENSP00000471041.1:n.*1355A>G
ENST00000376716.9:c.*1355A>G ENSP00000365906.4:n.*1355A>G
ENST00000594083.5:c.*1355A>G ENSP00000471549.1:n.*1355A>G
ENST00000599177.5:c.*3374A>G ENSP00000470475.1:n.*3374A>G
ENST00000602063.5:c.*1355A>G ENSP00000473089.1:n.*1355A>G
NM_001199324.1:c.*1355A>G NP_001186253.1:n.*1355A>G
NM_198480.3:c.*1355A>G NP_940882.3:n.*1355A>G
XM_011526822.1:c.*1355A>G XP_011525124.1:n.*1355A>G
XM_011526823.1:c.*1355A>G XP_011525125.1:n.*1355A>G
XM_011526824.1:c.*1355A>G XP_011525126.1:n.*1355A>G
XM_011526825.1:c.*1355A>G XP_011525127.1:n.*1355A>G
XM_011526826.1:c.*1355A>G XP_011525128.1:n.*1355A>G
XM_011526827.1:c.*1355A>G XP_011525129.1:n.*1355A>G
XM_011526828.1:c.*1355A>G XP_011525130.1:n.*1355A>G
XM_011526829.1:c.*1355A>G XP_011525131.1:n.*1355A>G
XM_011526830.1:c.*1355A>G XP_011525132.1:n.*1355A>G
XM_011526831.1:c.*1355A>G XP_011525133.1:n.*1355A>G
NM_001321317.1:c.*1355A>G NP_001308246.1:n.*1355A>G
NM_001321318.1:c.*1355A>G NP_001308247.1:n.*1355A>G
NM_001321319.1:c.*1355A>G NP_001308248.1:n.*1355A>G
NM_001321320.1:c.*1355A>G NP_001308249.1:n.*1355A>G
NM_001321321.1:c.*1355A>G NP_001308250.1:n.*1355A>G
NM_001321322.1:c.*1355A>G NP_001308251.1:n.*1355A>G
NM_001321323.1:c.*1355A>G NP_001308252.1:n.*1355A>G
XM_011526829.2:c.*1355A>G XP_011525131.1:n.*1355A>G
XM_017026648.2:c.*1355A>G XP_016882137.1:n.*1355A>G
XM_017026649.2:c.*1355A>G XP_016882138.1:n.*1355A>G
XM_017026650.2:c.*1355A>G XP_016882139.1:n.*1355A>G
XM_017026651.2:c.*1355A>G XP_016882140.1:n.*1355A>G
NM_001199324.2:c.*1355A>G MANE Select NP_001186253.1:n.*1355A>G
NM_001321317.2:c.*1355A>G NP_001308246.1:n.*1355A>G
NM_001321318.2:c.*1355A>G NP_001308247.1:n.*1355A>G
NM_001321319.2:c.*1355A>G NP_001308248.1:n.*1355A>G
NM_001321320.2:c.*1355A>G NP_001308249.1:n.*1355A>G
NM_001321321.2:c.*1355A>G NP_001308250.1:n.*1355A>G
NM_001321322.2:c.*1355A>G NP_001308251.1:n.*1355A>G
NM_001321323.2:c.*1355A>G NP_001308252.1:n.*1355A>G
NM_198480.4:c.*1355A>G NP_940882.3:n.*1355A>G
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