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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:
CA399966585
Gene: NOG
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2663770
ClinVar RCV Id:
RCV003884004
MyVariant Identifiers:
chr17:g.54672137T>C (hg19)
chr17:g.56594776T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.56594776T>C , CM000679.2:g.56594776T>C
GRCh38
NC_000017.10:g.54672137T>C , CM000679.1:g.54672137T>C
GRCh37
NC_000017.9:g.52027136T>C
NCBI36
NG_011958.1:g.6078T>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000332822.6:c.553T>C
MANE Select
ENSP00000328181.4:p.Ser185Pro
ENST00000332822.4:c.553T>C
ENSP00000328181.4:p.Ser185Pro
NM_005450.4:c.553T>C
NP_005441.1:p.Ser185Pro
NM_005450.6:c.553T>C
MANE Select
NP_005441.1:p.Ser185Pro
Search 100 bp 5'
Search 100 bp 3'