Canonical Allele Identifier: CA769340665

Gene: EPAS1

Linked Data

• dbSNP Id: rs1260924176
• MyVariant Identifiers: chr2:g.46533286A>C (hg19) ; chr2:g.46306147A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46306147A>C , CM000664.2:g.46306147A>C	GRCh38
NC_000002.11:g.46533286A>C , CM000664.1:g.46533286A>C	GRCh37
NC_000002.10:g.46386790A>C	NCBI36
NG_016000.1:g.13746A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263734.5:c.26+8210A>C MANE Select	ENSP00000263734.3:n.26+8210A>C
ENST00000263734.4:c.26+8210A>C	ENSP00000263734.3:n.26+8210A>C
ENST00000449347.5:c.26+8210A>C	ENSP00000406137.1:n.26+8210A>C
ENST00000460015.1:n.432+12049A>C
ENST00000467888.5:n.174+8210A>C
NM_001430.4:c.26+8210A>C	NP_001421.2:n.26+8210A>C
XR_940055.1:n.2501+7946T>G
NM_001430.5:c.26+8210A>C MANE Select	NP_001421.2:n.26+8210A>C