LDH info

Canonical Allele Identifier: CA11185014
Gene: EPAS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10187368

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46350505G>A , CM000664.2:g.46350505G>A GRCh38
NC_000002.11:g.46577644G>A , CM000664.1:g.46577644G>A GRCh37
NC_000002.10:g.46431148G>A NCBI36
NG_016000.1:g.58104G>A

Transcript Alleles

HGVS Amino-acid change
NM_001430.4:c.217+3442G>A VV NP_001421.2:p.=
XM_011532698.1:c.256+3442G>A XP_011531000.1:p.=
XM_011532698.2:c.256+3442G>A XP_011531000.1:p.=
NM_001430.5:c.217+3442G>A VV MANE Preferred NP_001421.2:p.=
ENST00000263734.4:c.217+3442G>A ENSP00000263734.3:p.=
ENST00000449347.5:c.217+3442G>A ENSP00000406137.1:p.=
ENST00000475822.1:n.408+3442G>A