Canonical Allele Identifier: CA532297184

Gene: EPAS1

Linked Data

• dbSNP Id: rs1338139668
• gnomAD v2: 2-46556281-T-A
• gnomAD v3: 2-46329142-T-A
• gnomAD v4: 2-46329142-T-A
• MyVariant Identifiers: chr2:g.46556281T>A (hg19) ; chr2:g.46329142T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46329142T>A , CM000664.2:g.46329142T>A	GRCh38
NC_000002.11:g.46556281T>A , CM000664.1:g.46556281T>A	GRCh37
NC_000002.10:g.46409785T>A	NCBI36
NG_016000.1:g.36741T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263734.5:c.27-17731T>A MANE Select	ENSP00000263734.3:n.27-17731T>A
ENST00000263734.4:c.27-17731T>A	ENSP00000263734.3:n.27-17731T>A
ENST00000449347.5:c.27-17731T>A	ENSP00000406137.1:n.27-17731T>A
ENST00000460015.1:n.433-17731T>A
ENST00000467888.5:n.175-17731T>A
NM_001430.4:c.27-17731T>A	NP_001421.2:n.27-17731T>A
XM_011532698.1:c.65+3266T>A	XP_011531000.1:n.65+3266T>A
XR_940055.1:n.2355+6642A>T
XM_011532698.2:c.65+3266T>A	XP_011531000.1:n.65+3266T>A
NM_001430.5:c.27-17731T>A MANE Select	NP_001421.2:n.27-17731T>A