Canonical Allele Identifier: CA2495256705
Gene: EPAS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46329107G= , CM000664.2:g.46329107G= GRCh38
NC_000002.11:g.46556246G= , CM000664.1:g.46556246G= GRCh37
NC_000002.10:g.46409750G= NCBI36
NG_016000.1:g.36706G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263734.5:c.27-17766G= MANE Select ENSP00000263734.3:n.27-17766G=
ENST00000263734.4:c.27-17766G= ENSP00000263734.3:n.27-17766G=
ENST00000449347.5:c.27-17766G= ENSP00000406137.1:n.27-17766G=
ENST00000460015.1:n.433-17766G=
ENST00000467888.5:n.175-17766G=
NM_001430.4:c.27-17766G= NP_001421.2:n.27-17766G=
XM_011532698.1:c.65+3231G= XP_011531000.1:n.65+3231G=
XR_940055.1:n.2355+6677C=
XM_011532698.2:c.65+3231G= XP_011531000.1:n.65+3231G=
NM_001430.5:c.27-17766G= MANE Select NP_001421.2:n.27-17766G=
Search 100 bp 5'
Search 100 bp 3'