Canonical Allele Identifier: CA8283098
Gene: PAFAH1B1 HGNC NCBI

Linked Data

dbSNP Id: rs771951756
gnomAD v2: 17-2568704-A-G
gnomAD v4: 17-2665410-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2665410A>G , CM000679.2:g.2665410A>G GRCh38
NC_000017.10:g.2568704A>G , CM000679.1:g.2568704A>G GRCh37
NC_000017.9:g.2515454A>G NCBI36
NG_009799.1:g.76782A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.71A>G MANE Select ENSP00000380378.4:p.Tyr24Cys
ENST00000674608.1:c.125A>G ENSP00000501976.1:p.Tyr42Cys
ENST00000674717.1:c.-3-1582A>G ENSP00000501931.1:n.-3-1582A>G
ENST00000675202.1:c.71A>G ENSP00000502843.1:p.Tyr24Cys
ENST00000675331.1:c.71A>G ENSP00000502031.1:p.Tyr24Cys
ENST00000675390.1:c.71A>G ENSP00000501969.1:p.Tyr24Cys
ENST00000675430.1:n.298A>G
ENST00000675621.1:c.71A>G ENSP00000502117.1:p.Tyr24Cys
ENST00000675764.1:c.*25A>G ENSP00000502242.1:n.*25A>G
ENST00000676077.1:c.-125A>G ENSP00000502507.1:n.-125A>G
ENST00000676098.1:c.71A>G ENSP00000502735.1:p.Tyr24Cys
ENST00000676188.1:c.71A>G ENSP00000502577.1:p.Tyr24Cys
ENST00000676201.1:n.272-606A>G
ENST00000676353.1:c.-78-606A>G ENSP00000502737.1:n.-78-606A>G
ENST00000676456.1:n.223-606A>G
ENST00000397195.9:c.71A>G ENSP00000380378.4:p.Tyr24Cys
ENST00000570400.1:c.33-606A>G ENSP00000460258.1:n.33-606A>G
ENST00000572915.6:n.273-1582A>G
ENST00000574816.5:n.31-10904A>G
ENST00000575477.5:n.620-606A>G
ENST00000576586.5:c.71A>G ENSP00000461087.1:p.Tyr24Cys
ENST00000609078.1:n.30A>G
NM_000430.3:c.71A>G NP_000421.1:p.Tyr24Cys
XM_011523901.1:c.125A>G XP_011522203.1:p.Tyr42Cys
XM_011523902.1:c.125A>G XP_011522204.1:p.Tyr42Cys
XM_011523903.1:c.125A>G XP_011522205.1:p.Tyr42Cys
XM_011523904.1:c.125A>G XP_011522206.1:p.Tyr42Cys
XM_011523901.2:c.125A>G XP_011522203.1:p.Tyr42Cys
XM_011523902.3:c.125A>G XP_011522204.1:p.Tyr42Cys
XM_011523903.2:c.125A>G XP_011522205.1:p.Tyr42Cys
XM_017024701.1:c.71A>G XP_016880190.1:p.Tyr24Cys
XM_017024702.2:c.-78-606A>G XP_016880191.1:n.-78-606A>G
NM_000430.4:c.71A>G MANE Select NP_000421.1:p.Tyr24Cys