Canonical Allele Identifier: CA359307495
Gene: PRDM9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.23509147G>C (hg19) chr5:g.23509038G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.23509038G>C , CM000667.2:g.23509038G>C GRCh38
NC_000005.9:g.23509147G>C , CM000667.1:g.23509147G>C GRCh37
NC_000005.8:g.23544904G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502755.6:c.5G>C ENSP00000425471.2:p.Ser2Thr
ENST00000296682.4:c.5G>C MANE Select ENSP00000296682.4:p.Ser2Thr
ENST00000296682.3:c.5G>C ENSP00000296682.3:p.Ser2Thr
ENST00000502755.5:c.5G>C ENSP00000425471.1:p.Ser2Thr
ENST00000635252.1:c.17-882G>C ENSP00000489227.1:n.17-882G>C
NM_020227.2:c.5G>C NP_064612.2:p.Ser2Thr
NM_020227.3:c.5G>C NP_064612.2:p.Ser2Thr
NM_001376900.1:c.5G>C NP_001363829.1:p.Ser2Thr
NM_020227.4:c.5G>C MANE Select NP_064612.2:p.Ser2Thr
Search 100 bp 5'
Search 100 bp 3'