Canonical Allele Identifier: CA397638384
Gene: PAFAH1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1177684964
gnomAD v2: 17-2569340-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2666046C>G , CM000679.2:g.2666046C>G GRCh38
NC_000017.10:g.2569340C>G , CM000679.1:g.2569340C>G GRCh37
NC_000017.9:g.2516090C>G NCBI36
NG_009799.1:g.77418C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.148C>G MANE Select ENSP00000380378.4:p.Leu50Val
ENST00000674608.1:c.202C>G ENSP00000501976.1:p.Leu68Val
ENST00000674717.1:c.-3-946C>G ENSP00000501931.1:n.-3-946C>G
ENST00000675202.1:c.148C>G ENSP00000502843.1:p.Leu50Val
ENST00000675331.1:c.148C>G ENSP00000502031.1:p.Leu50Val
ENST00000675390.1:c.148C>G ENSP00000501969.1:p.Leu50Val
ENST00000675430.1:n.375C>G
ENST00000675621.1:c.148C>G ENSP00000502117.1:p.Leu50Val
ENST00000675764.1:c.*102C>G ENSP00000502242.1:n.*102C>G
ENST00000676077.1:c.-48C>G ENSP00000502507.1:n.-48C>G
ENST00000676098.1:c.148C>G ENSP00000502735.1:p.Leu50Val
ENST00000676188.1:c.148C>G ENSP00000502577.1:p.Leu50Val
ENST00000676201.1:n.302C>G
ENST00000676353.1:c.-48C>G ENSP00000502737.1:n.-48C>G
ENST00000676456.1:n.253C>G
ENST00000397195.9:c.148C>G ENSP00000380378.4:p.Leu50Val
ENST00000570400.1:c.*18C>G ENSP00000460258.1:n.*18C>G
ENST00000572915.6:n.273-946C>G
ENST00000574816.5:n.31-10268C>G
ENST00000575477.5:n.650C>G
ENST00000576586.5:c.148C>G ENSP00000461087.1:p.Leu50Val
ENST00000609078.1:n.107C>G
NM_000430.3:c.148C>G NP_000421.1:p.Leu50Val
XM_011523901.1:c.202C>G XP_011522203.1:p.Leu68Val
XM_011523902.1:c.202C>G XP_011522204.1:p.Leu68Val
XM_011523903.1:c.202C>G XP_011522205.1:p.Leu68Val
XM_011523904.1:c.202C>G XP_011522206.1:p.Leu68Val
XM_011523901.2:c.202C>G XP_011522203.1:p.Leu68Val
XM_011523902.3:c.202C>G XP_011522204.1:p.Leu68Val
XM_011523903.2:c.202C>G XP_011522205.1:p.Leu68Val
XM_017024701.1:c.148C>G XP_016880190.1:p.Leu50Val
XM_017024702.2:c.-48C>G XP_016880191.1:n.-48C>G
NM_000430.4:c.148C>G MANE Select NP_000421.1:p.Leu50Val