Canonical Allele Identifier: CA769354194

Gene: EPAS1

Linked Data

• dbSNP Id: rs1460608488
• MyVariant Identifiers: chr2:g.46556337A>T (hg19) ; chr2:g.46329198A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46329198A>T , CM000664.2:g.46329198A>T	GRCh38
NC_000002.11:g.46556337A>T , CM000664.1:g.46556337A>T	GRCh37
NC_000002.10:g.46409841A>T	NCBI36
NG_016000.1:g.36797A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263734.5:c.27-17675A>T MANE Select	ENSP00000263734.3:n.27-17675A>T
ENST00000263734.4:c.27-17675A>T	ENSP00000263734.3:n.27-17675A>T
ENST00000449347.5:c.27-17675A>T	ENSP00000406137.1:n.27-17675A>T
ENST00000460015.1:n.433-17675A>T
ENST00000467888.5:n.175-17675A>T
NM_001430.4:c.27-17675A>T	NP_001421.2:n.27-17675A>T
XM_011532698.1:c.65+3322A>T	XP_011531000.1:n.65+3322A>T
XR_940055.1:n.2355+6586T>A
XM_011532698.2:c.65+3322A>T	XP_011531000.1:n.65+3322A>T
NM_001430.5:c.27-17675A>T MANE Select	NP_001421.2:n.27-17675A>T