Canonical Allele Identifier: CA2495245886
Gene: EPAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46306269T= , CM000664.2:g.46306269T= GRCh38
NC_000002.11:g.46533408T= , CM000664.1:g.46533408T= GRCh37
NC_000002.10:g.46386912T= NCBI36
NG_016000.1:g.13868T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263734.5:c.26+8332T= MANE Select ENSP00000263734.3:n.26+8332T=
ENST00000263734.4:c.26+8332T= ENSP00000263734.3:n.26+8332T=
ENST00000449347.5:c.26+8332T= ENSP00000406137.1:n.26+8332T=
ENST00000460015.1:n.432+12171T=
ENST00000467888.5:n.174+8332T=
NM_001430.4:c.26+8332T= NP_001421.2:n.26+8332T=
XR_940055.1:n.2501+7824A=
NM_001430.5:c.26+8332T= MANE Select NP_001421.2:n.26+8332T=