Canonical Allele Identifier: CA1030172010
Gene: EPAS1 HGNC NCBI

Linked Data

dbSNP Id: rs1683106510
gnomAD v3: 2-46306208-T-C
gnomAD v4: 2-46306208-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46306208T>C , CM000664.2:g.46306208T>C GRCh38
NC_000002.11:g.46533347T>C , CM000664.1:g.46533347T>C GRCh37
NC_000002.10:g.46386851T>C NCBI36
NG_016000.1:g.13807T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263734.5:c.26+8271T>C MANE Select ENSP00000263734.3:n.26+8271T>C
ENST00000263734.4:c.26+8271T>C ENSP00000263734.3:n.26+8271T>C
ENST00000449347.5:c.26+8271T>C ENSP00000406137.1:n.26+8271T>C
ENST00000460015.1:n.432+12110T>C
ENST00000467888.5:n.174+8271T>C
NM_001430.4:c.26+8271T>C NP_001421.2:n.26+8271T>C
XR_940055.1:n.2501+7885A>G
NM_001430.5:c.26+8271T>C MANE Select NP_001421.2:n.26+8271T>C