Canonical Allele Identifier: CA2495245857
Gene: EPAS1 HGNC NCBI

Linked Data

dbSNP Id: rs1683106455

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46306203T>C , CM000664.2:g.46306203T>C GRCh38
NC_000002.11:g.46533342T>C , CM000664.1:g.46533342T>C GRCh37
NC_000002.10:g.46386846T>C NCBI36
NG_016000.1:g.13802T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263734.5:c.26+8266T>C MANE Select ENSP00000263734.3:n.26+8266T>C
ENST00000263734.4:c.26+8266T>C ENSP00000263734.3:n.26+8266T>C
ENST00000449347.5:c.26+8266T>C ENSP00000406137.1:n.26+8266T>C
ENST00000460015.1:n.432+12105T>C
ENST00000467888.5:n.174+8266T>C
NM_001430.4:c.26+8266T>C NP_001421.2:n.26+8266T>C
XR_940055.1:n.2501+7890A>G
NM_001430.5:c.26+8266T>C MANE Select NP_001421.2:n.26+8266T>C