Canonical Allele Identifier: CA769367716
Gene: EPAS1 HGNC NCBI

Linked Data

dbSNP Id: rs918157436

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46350431G>T , CM000664.2:g.46350431G>T GRCh38
NC_000002.11:g.46577570G>T , CM000664.1:g.46577570G>T GRCh37
NC_000002.10:g.46431074G>T NCBI36
NG_016000.1:g.58030G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263734.5:c.217+3368G>T MANE Select ENSP00000263734.3:n.217+3368G>T
ENST00000263734.4:c.217+3368G>T ENSP00000263734.3:n.217+3368G>T
ENST00000449347.5:c.217+3368G>T ENSP00000406137.1:n.217+3368G>T
ENST00000475822.1:n.408+3368G>T
NM_001430.4:c.217+3368G>T NP_001421.2:n.217+3368G>T
XM_011532698.1:c.256+3368G>T XP_011531000.1:n.256+3368G>T
XM_011532698.2:c.256+3368G>T XP_011531000.1:n.256+3368G>T
NM_001430.5:c.217+3368G>T MANE Select NP_001421.2:n.217+3368G>T