Canonical Allele Identifier: CA449767589
Gene: RNF39 HGNC NCBI

Linked Data

gnomAD v4: 6-30071474-A-T
MyVariant Identifiers: chr6:g.30039251A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30071474A>T , CM000668.2:g.30071474A>T GRCh38
NC_000006.11:g.30039251A>T , CM000668.1:g.30039251A>T GRCh37
NC_000006.10:g.30147230A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244360.8:c.696T>A MANE Select ENSP00000244360.7:p.Ser232=
ENST00000244360.7:c.696T>A ENSP00000244360.7:p.Ser232=
ENST00000376751.8:c.696T>A ENSP00000365942.4:p.Ser232=
ENST00000244360.6:c.900T>A ENSP00000244360.6:p.Ser300=
ENST00000376751.7:c.900T>A ENSP00000365942.3:p.Ser300=
NM_025236.3:c.900T>A NP_079512.2:p.Ser300=
NM_170769.2:c.900T>A NP_739575.2:p.Ser300=
XM_017011325.1:c.441T>A XP_016866814.1:p.Ser147=
NM_025236.4:c.696T>A MANE Select NP_079512.3:p.Ser232=
NM_170769.3:c.696T>A NP_739575.3:p.Ser232=
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Search 100 bp 3'