Canonical Allele Identifier: CA8283216

Gene: PAFAH1B1

Linked Data

• dbSNP Id: rs759203616
• ExAC: 17:2575907 G / A
• gnomAD v2: 17-2575907-G-A
• gnomAD v4: 17-2672613-G-A
• MyVariant Identifiers: chr17:g.2575907G>A (hg19) ; chr17:g.2672613G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2672613G>A , CM000679.2:g.2672613G>A	GRCh38
NC_000017.10:g.2575907G>A , CM000679.1:g.2575907G>A	GRCh37
NC_000017.9:g.2522657G>A	NCBI36
NG_009799.1:g.83985G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.569-42G>A MANE Select	ENSP00000380378.4:n.569-42G>A
ENST00000571495.2:n.310G>A
ENST00000674608.1:c.623-42G>A	ENSP00000501976.1:n.623-42G>A
ENST00000674717.1:c.374-42G>A	ENSP00000501931.1:n.374-42G>A
ENST00000675202.1:c.569-42G>A	ENSP00000502843.1:n.569-42G>A
ENST00000675331.1:c.569-42G>A	ENSP00000502031.1:n.569-42G>A
ENST00000675390.1:c.569-42G>A	ENSP00000501969.1:n.569-42G>A
ENST00000675574.1:n.297G>A
ENST00000675621.1:c.569-42G>A	ENSP00000502117.1:n.569-42G>A
ENST00000675764.1:c.*523-42G>A	ENSP00000502242.1:n.*523-42G>A
ENST00000676077.1:c.374-1447G>A	ENSP00000502507.1:n.374-1447G>A
ENST00000676098.1:c.569-42G>A	ENSP00000502735.1:n.569-42G>A
ENST00000676188.1:c.569-42G>A	ENSP00000502577.1:n.569-42G>A
ENST00000676353.1:c.374-42G>A	ENSP00000502737.1:n.374-42G>A
ENST00000397193.7:n.377-42G>A
ENST00000397195.9:c.569-42G>A	ENSP00000380378.4:n.569-42G>A
ENST00000572915.6:n.537-42G>A
ENST00000574468.1:c.65-42G>A	ENSP00000460591.1:n.65-42G>A
ENST00000574816.5:n.31-3701G>A
NM_000430.3:c.569-42G>A	NP_000421.1:n.569-42G>A
XM_011523901.1:c.623-42G>A	XP_011522203.1:n.623-42G>A
XM_011523902.1:c.623-42G>A	XP_011522204.1:n.623-42G>A
XM_011523903.1:c.623-42G>A	XP_011522205.1:n.623-42G>A
XM_011523904.1:c.623-1447G>A	XP_011522206.1:n.623-1447G>A
XM_011523901.2:c.623-42G>A	XP_011522203.1:n.623-42G>A
XM_011523902.3:c.623-42G>A	XP_011522204.1:n.623-42G>A
XM_011523903.2:c.623-42G>A	XP_011522205.1:n.623-42G>A
XM_017024701.1:c.569-42G>A	XP_016880190.1:n.569-42G>A
XM_017024702.2:c.374-42G>A	XP_016880191.1:n.374-42G>A
NM_000430.4:c.569-42G>A MANE Select	NP_000421.1:n.569-42G>A