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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA1645387
Gene: EPAS1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
336282
ClinVar RCV Id:
RCV000378133
RCV000964860
dbSNP Id:
rs35795449
ExAC:
2:46611697 C / T
gnomAD v2:
2-46611697-C-T
gnomAD v3:
2-46384558-C-T
gnomAD v4:
2-46384558-C-T
MyVariant Identifiers:
chr2:g.46611697C>T (hg19)
chr2:g.46384558C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.46384558C>T , CM000664.2:g.46384558C>T
GRCh38
NC_000002.11:g.46611697C>T , CM000664.1:g.46611697C>T
GRCh37
NC_000002.10:g.46465201C>T
NCBI36
NG_016000.1:g.92157C>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000263734.5:c.2511C>T
MANE Select
ENSP00000263734.3:p.Pro837=
ENST00000263734.4:c.2511C>T
ENSP00000263734.3:p.Pro837=
ENST00000466465.5:n.1484C>T
NM_001430.4:c.2511C>T
NP_001421.2:p.Pro837=
XM_011532698.1:c.2550C>T
XP_011531000.1:p.Pro850=
XM_011532698.2:c.2550C>T
XP_011531000.1:p.Pro850=
NM_001430.5:c.2511C>T
MANE Select
NP_001421.2:p.Pro837=
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