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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:
CA275629
Gene: AGXT
HGNC
NCBI
Linked Data
ClinVar Variation Id:
204073
ClinVar RCV Id:
RCV000186279
dbSNP Id:
rs180177168
gnomAD v2:
2-241808404-G-A
gnomAD v3:
2-240868987-G-A
gnomAD v4:
2-240868987-G-A
MyVariant Identifiers:
chr2:g.241808404G>A (hg19)
chr2:g.240868987G>A (hg38)
PubMed:
PMID:17495019
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.240868987G>A , CM000664.2:g.240868987G>A
GRCh38
NC_000002.11:g.241808404G>A , CM000664.1:g.241808404G>A
GRCh37
NC_000002.10:g.241457077G>A
NCBI36
NG_008005.1:g.5243G>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000307503.4:c.122G>A
MANE Select
ENSP00000302620.3:p.Gly41Glu
ENST00000307503.3:c.122G>A
ENSP00000302620.3:p.Gly41Glu
ENST00000472436.1:n.142G>A
NM_000030.2:c.122G>A
NP_000021.1:p.Gly41Glu
XR_924060.1:n.405+1246C>T
NM_000030.3:c.122G>A
MANE Select
NP_000021.1:p.Gly41Glu
Search 100 bp 5'
Search 100 bp 3'