Canonical Allele Identifier: CA2495257388
Gene: EPAS1 HGNC NCBI

Linked Data

dbSNP Id: rs1683652303

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46330471G>A , CM000664.2:g.46330471G>A GRCh38
NC_000002.11:g.46557610G>A , CM000664.1:g.46557610G>A GRCh37
NC_000002.10:g.46411114G>A NCBI36
NG_016000.1:g.38070G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263734.5:c.27-16402G>A MANE Select ENSP00000263734.3:n.27-16402G>A
ENST00000263734.4:c.27-16402G>A ENSP00000263734.3:n.27-16402G>A
ENST00000449347.5:c.27-16402G>A ENSP00000406137.1:n.27-16402G>A
ENST00000460015.1:n.433-16402G>A
ENST00000467888.5:n.175-16402G>A
NM_001430.4:c.27-16402G>A NP_001421.2:n.27-16402G>A
XM_011532698.1:c.65+4595G>A XP_011531000.1:n.65+4595G>A
XR_940055.1:n.2355+5313C>T
XM_011532698.2:c.65+4595G>A XP_011531000.1:n.65+4595G>A
NM_001430.5:c.27-16402G>A MANE Select NP_001421.2:n.27-16402G>A