Canonical Allele Identifier: CA2699319129
Gene: EPAS1 HGNC NCBI

Linked Data

dbSNP Id: rs2104838162

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46306277T>A , CM000664.2:g.46306277T>A GRCh38
NC_000002.11:g.46533416T>A , CM000664.1:g.46533416T>A GRCh37
NC_000002.10:g.46386920T>A NCBI36
NG_016000.1:g.13876T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263734.5:c.26+8340T>A MANE Select ENSP00000263734.3:n.26+8340T>A
ENST00000263734.4:c.26+8340T>A ENSP00000263734.3:n.26+8340T>A
ENST00000449347.5:c.26+8340T>A ENSP00000406137.1:n.26+8340T>A
ENST00000460015.1:n.432+12179T>A
ENST00000467888.5:n.174+8340T>A
NM_001430.4:c.26+8340T>A NP_001421.2:n.26+8340T>A
XR_940055.1:n.2501+7816A>T
NM_001430.5:c.26+8340T>A MANE Select NP_001421.2:n.26+8340T>A