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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:
CA409101687
Gene: JPH2
HGNC
NCBI
Linked Data
dbSNP Id:
rs1222315380
gnomAD v3:
20-44118519-T-C
gnomAD v4:
20-44118519-T-C
MyVariant Identifiers:
chr20:g.42747159T>C (hg19)
chr20:g.44118519T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.44118519T>C , CM000682.2:g.44118519T>C
GRCh38
NC_000020.10:g.42747159T>C , CM000682.1:g.42747159T>C
GRCh37
NC_000020.9:g.42180573T>C
NCBI36
NG_031867.1:g.74060A>G , LRG_394:g.74060A>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000372980.4:c.1274A>G
MANE Select
ENSP00000362071.3:p.Asp425Gly
ENST00000372980.3:c.1274A>G
ENSP00000362071.3:p.Asp425Gly
NM_020433.4:c.1274A>G , LRG_394t1:c.1274A>G
NP_065166.2:p.Asp425Gly
XM_006723832.2:c.1274A>G
XP_006723895.1:p.Asp425Gly
NM_020433.5:c.1274A>G
MANE Select
NP_065166.2:p.Asp425Gly
Search 100 bp 5'
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