Canonical Allele Identifier: CA10639186

Gene: PAFAH1B1

Linked Data

• dbSNP Id: rs563543268
• gnomAD v3: 17-2638227-T-G
• gnomAD v4: 17-2638227-T-G
• MyVariant Identifiers: chr17:g.2541521T>G (hg19) ; chr17:g.2638227T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2638227T>G , CM000679.2:g.2638227T>G	GRCh38
NC_000017.10:g.2541521T>G , CM000679.1:g.2541521T>G	GRCh37
NC_000017.9:g.2488271T>G	NCBI36
NG_009799.1:g.49599T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000397195.10:c.-62T>G MANE Select	ENSP00000380378.4:n.-62T>G
ENST00000674608.1:c.-62T>G	ENSP00000501976.1:n.-62T>G
ENST00000674717.1:c.-97T>G	ENSP00000501931.1:n.-97T>G
ENST00000675202.1:c.-62T>G	ENSP00000502843.1:n.-62T>G
ENST00000675331.1:c.-62T>G	ENSP00000502031.1:n.-62T>G
ENST00000675390.1:c.-62T>G	ENSP00000501969.1:n.-62T>G
ENST00000675430.1:n.166T>G
ENST00000675621.1:c.-62T>G	ENSP00000502117.1:n.-62T>G
ENST00000675764.1:c.-62T>G	ENSP00000502242.1:n.-62T>G
ENST00000676077.1:c.-163-27145T>G	ENSP00000502507.1:n.-163-27145T>G
ENST00000676098.1:c.-62T>G	ENSP00000502735.1:n.-62T>G
ENST00000676188.1:c.-62T>G	ENSP00000502577.1:n.-62T>G
ENST00000676201.1:n.178T>G
ENST00000676353.1:c.-172T>G	ENSP00000502737.1:n.-172T>G
ENST00000676456.1:n.129T>G
ENST00000397195.9:c.-62T>G	ENSP00000380378.4:n.-62T>G
ENST00000570400.1:c.-62T>G	ENSP00000460258.1:n.-62T>G
ENST00000571289.1:n.168T>G
ENST00000572915.6:n.179T>G
ENST00000574816.5:n.30+28659T>G
ENST00000575477.5:n.526T>G
ENST00000576586.5:c.-62T>G	ENSP00000461087.1:n.-62T>G
NM_000430.3:c.-62T>G	NP_000421.1:n.-62T>G
XM_011523901.1:c.-62T>G	XP_011522203.1:n.-62T>G
XM_011523902.1:c.-62T>G	XP_011522204.1:n.-62T>G
XM_011523903.1:c.-62T>G	XP_011522205.1:n.-62T>G
XM_011523904.1:c.-62T>G	XP_011522206.1:n.-62T>G
XM_011523901.2:c.-62T>G	XP_011522203.1:n.-62T>G
XM_011523902.3:c.-62T>G	XP_011522204.1:n.-62T>G
XM_011523903.2:c.-62T>G	XP_011522205.1:n.-62T>G
XM_017024701.1:c.-62T>G	XP_016880190.1:n.-62T>G
XM_017024702.2:c.-172T>G	XP_016880191.1:n.-172T>G
NM_000430.4:c.-62T>G MANE Select	NP_000421.1:n.-62T>G