Canonical Allele Identifier: CA2699318896
Gene: EPAS1 HGNC NCBI

Linked Data

dbSNP Id: rs2104838158

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46306272A>G , CM000664.2:g.46306272A>G GRCh38
NC_000002.11:g.46533411A>G , CM000664.1:g.46533411A>G GRCh37
NC_000002.10:g.46386915A>G NCBI36
NG_016000.1:g.13871A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263734.5:c.26+8335A>G MANE Select ENSP00000263734.3:n.26+8335A>G
ENST00000263734.4:c.26+8335A>G ENSP00000263734.3:n.26+8335A>G
ENST00000449347.5:c.26+8335A>G ENSP00000406137.1:n.26+8335A>G
ENST00000460015.1:n.432+12174A>G
ENST00000467888.5:n.174+8335A>G
NM_001430.4:c.26+8335A>G NP_001421.2:n.26+8335A>G
XR_940055.1:n.2501+7821T>C
NM_001430.5:c.26+8335A>G MANE Select NP_001421.2:n.26+8335A>G