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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:
CA518287076
Gene: AGTR2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrX:g.115304553C>T (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.116173300C>T , CM000685.2:g.116173300C>T
GRCh38
NC_000023.10:g.115304553C>T , CM000685.1:g.115304553C>T
GRCh37
NC_000023.9:g.115218581C>T
NCBI36
NG_016326.1:g.7596C>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000371906.5:c.1020C>T
MANE Select
ENSP00000360973.4:p.Leu340=
ENST00000680409.1:n.1488C>T
ENST00000681852.1:c.1020C>T
ENSP00000505750.1:p.Leu340=
ENST00000371906.4:c.1020C>T
ENSP00000360973.4:p.Leu340=
NM_000686.4:c.1020C>T
NP_000677.2:p.Leu340=
XM_011537533.1:c.1020C>T
XP_011535835.1:p.Leu340=
NM_000686.5:c.1020C>T
MANE Select
NP_000677.2:p.Leu340=
NM_001385624.1:c.1020C>T
NP_001372553.1:p.Leu340=
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