Canonical Allele Identifier: CA15609812
Gene: ZNF483 HGNC NCBI

Linked Data

dbSNP Id: rs10441737

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111539305C>T , CM000671.2:g.111539305C>T GRCh38
NC_000009.11:g.114301585C>T , CM000671.1:g.114301585C>T GRCh37
NC_000009.10:g.113341406C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000309235.6:c.722-2352C>T MANE Select ENSP00000311679.5:n.722-2352C>T
ENST00000309235.5:c.722-2352C>T ENSP00000311679.5:n.722-2352C>T
ENST00000355824.7:c.722-141C>T ENSP00000438048.1:n.722-141C>T
ENST00000358151.8:c.721+4952C>T ENSP00000350871.4:n.721+4952C>T
NM_001007169.3:c.721+4952C>T NP_001007170.1:n.721+4952C>T
NM_133464.3:c.722-2352C>T NP_597721.2:n.722-2352C>T
XM_011518299.1:c.722-2352C>T XP_011516601.1:n.722-2352C>T
XM_011518300.1:c.722-2352C>T XP_011516602.1:n.722-2352C>T
XM_011518301.1:c.254-2352C>T XP_011516603.1:n.254-2352C>T
NM_001007169.4:c.721+4952C>T NP_001007170.1:n.721+4952C>T
NM_133464.4:c.722-2352C>T NP_597721.2:n.722-2352C>T
XM_011518300.2:c.722-2352C>T XP_011516602.1:n.722-2352C>T
XM_017014337.1:c.722-2352C>T XP_016869826.1:n.722-2352C>T
XM_017014338.1:c.722-2352C>T XP_016869827.1:n.722-2352C>T
XM_017014339.1:c.722-141C>T XP_016869828.1:n.722-141C>T
NM_001007169.5:c.721+4952C>T NP_001007170.1:n.721+4952C>T
NM_133464.5:c.722-2352C>T MANE Select NP_597721.2:n.722-2352C>T
NM_001007169.6:c.721+4952C>T NP_001007170.1:n.721+4952C>T