Canonical Allele Identifier: CA16607544
Gene: PAFAH1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 382036
ClinVar RCV Id: RCV000441930
dbSNP Id: rs1057521243

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2665371G>C , CM000679.2:g.2665371G>C GRCh38
NC_000017.10:g.2568665G>C , CM000679.1:g.2568665G>C GRCh37
NC_000017.9:g.2515415G>C NCBI36
NG_009799.1:g.76743G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000397195.10:c.33-1G>C MANE Select ENSP00000380378.4:n.33-1G>C
ENST00000674608.1:c.87-1G>C ENSP00000501976.1:n.87-1G>C
ENST00000674717.1:c.-3-1621G>C ENSP00000501931.1:n.-3-1621G>C
ENST00000675202.1:c.33-1G>C ENSP00000502843.1:n.33-1G>C
ENST00000675331.1:c.33-1G>C ENSP00000502031.1:n.33-1G>C
ENST00000675390.1:c.33-1G>C ENSP00000501969.1:n.33-1G>C
ENST00000675430.1:n.260-1G>C
ENST00000675621.1:c.33-1G>C ENSP00000502117.1:n.33-1G>C
ENST00000675764.1:c.131-1G>C ENSP00000502242.1:n.131-1G>C
ENST00000676077.1:c.-163-1G>C ENSP00000502507.1:n.-163-1G>C
ENST00000676098.1:c.33-1G>C ENSP00000502735.1:n.33-1G>C
ENST00000676188.1:c.33-1G>C ENSP00000502577.1:n.33-1G>C
ENST00000676201.1:n.272-645G>C
ENST00000676353.1:c.-78-645G>C ENSP00000502737.1:n.-78-645G>C
ENST00000676456.1:n.223-645G>C
ENST00000397195.9:c.33-1G>C ENSP00000380378.4:n.33-1G>C
ENST00000570400.1:c.33-645G>C ENSP00000460258.1:n.33-645G>C
ENST00000572915.6:n.273-1621G>C
ENST00000574816.5:n.31-10943G>C
ENST00000575477.5:n.620-645G>C
ENST00000576586.5:c.33-1G>C ENSP00000461087.1:n.33-1G>C
NM_000430.3:c.33-1G>C NP_000421.1:n.33-1G>C
XM_011523901.1:c.87-1G>C XP_011522203.1:n.87-1G>C
XM_011523902.1:c.87-1G>C XP_011522204.1:n.87-1G>C
XM_011523903.1:c.87-1G>C XP_011522205.1:n.87-1G>C
XM_011523904.1:c.87-1G>C XP_011522206.1:n.87-1G>C
XM_011523901.2:c.87-1G>C XP_011522203.1:n.87-1G>C
XM_011523902.3:c.87-1G>C XP_011522204.1:n.87-1G>C
XM_011523903.2:c.87-1G>C XP_011522205.1:n.87-1G>C
XM_017024701.1:c.33-1G>C XP_016880190.1:n.33-1G>C
XM_017024702.2:c.-78-645G>C XP_016880191.1:n.-78-645G>C
NM_000430.4:c.33-1G>C MANE Select NP_000421.1:n.33-1G>C