Canonical Allele Identifier: CA823780193

Gene: RNF39

Linked Data

• dbSNP Id: rs1210749415
• MyVariant Identifiers: chr6:g.30040768T>A (hg19) ; chr6:g.30072991T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30072991T>A , CM000668.2:g.30072991T>A	GRCh38
NC_000006.11:g.30040768T>A , CM000668.1:g.30040768T>A	GRCh37
NC_000006.10:g.30148747T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244360.8:c.478+166A>T MANE Select	ENSP00000244360.7:n.478+166A>T
ENST00000244360.7:c.478+166A>T	ENSP00000244360.7:n.478+166A>T
ENST00000376751.8:c.478+166A>T	ENSP00000365942.4:n.478+166A>T
ENST00000244360.6:c.682+166A>T	ENSP00000244360.6:n.682+166A>T
ENST00000376751.7:c.682+166A>T	ENSP00000365942.3:n.682+166A>T
NM_025236.3:c.682+166A>T	NP_079512.2:n.682+166A>T
NM_170769.2:c.682+166A>T	NP_739575.2:n.682+166A>T
XM_017011325.1:c.223+166A>T	XP_016866814.1:n.223+166A>T
XM_017011326.1:c.682+166A>T	XP_016866815.1:n.682+166A>T
NM_025236.4:c.478+166A>T MANE Select	NP_079512.3:n.478+166A>T
NM_170769.3:c.478+166A>T	NP_739575.3:n.478+166A>T