Canonical Allele Identifier: CA1030172009
Gene: EPAS1 HGNC NCBI

Linked Data

dbSNP Id: rs149697904
gnomAD v3: 2-46306207-A-G
gnomAD v4: 2-46306207-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46306207A>G , CM000664.2:g.46306207A>G GRCh38
NC_000002.11:g.46533346A>G , CM000664.1:g.46533346A>G GRCh37
NC_000002.10:g.46386850A>G NCBI36
NG_016000.1:g.13806A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263734.5:c.26+8270A>G MANE Select ENSP00000263734.3:n.26+8270A>G
ENST00000263734.4:c.26+8270A>G ENSP00000263734.3:n.26+8270A>G
ENST00000449347.5:c.26+8270A>G ENSP00000406137.1:n.26+8270A>G
ENST00000460015.1:n.432+12109A>G
ENST00000467888.5:n.174+8270A>G
NM_001430.4:c.26+8270A>G NP_001421.2:n.26+8270A>G
XR_940055.1:n.2501+7886T>C
NM_001430.5:c.26+8270A>G MANE Select NP_001421.2:n.26+8270A>G