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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:
CA211666230
Gene: CYP2C19
HGNC
NCBI
Linked Data
dbSNP Id:
rs377381376
gnomAD v4:
10-94762709-G-C
MyVariant Identifiers:
chr10:g.96522466G>C (hg19)
chr10:g.94762709G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.94762709G>C , CM000672.2:g.94762709G>C
GRCh38
NC_000010.10:g.96522466G>C , CM000672.1:g.96522466G>C
GRCh37
NC_000010.9:g.96512456G>C
NCBI36
NG_008384.2:g.5004G>C
NG_008384.3:g.5029G>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000371321.9:c.4G>C
MANE Select
ENSP00000360372.3:p.Asp2His
ENST00000371321.7:c.4G>C
ENSP00000360372.3:p.Asp2His
ENST00000464755.1:c.932-12349G>C
ENSP00000483243.1:n.932-12349G>C
ENST00000480405.2:c.4G>C
ENSP00000483847.1:p.Asp2His
NM_000769.2:c.4G>C
NP_000760.1:p.Asp2His
NM_000769.4:c.4G>C
MANE Select
NP_000760.1:p.Asp2His
Search 100 bp 5'
Search 100 bp 3'