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ClinGen Allele Registry
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Canonical Allele Identifier:
CA1929221642
Community Standard Title: NM_000769.4(CYP2C19):c.636G= (p.Trp212=)
Gene: CYP2C19
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.94780653G= , CM000672.2:g.94780653G=
GRCh38
NC_000010.10:g.96540410G= , CM000672.1:g.96540410G=
GRCh37
NC_000010.9:g.96530400G=
NCBI36
NG_008384.2:g.22948G=
NG_008384.3:g.22973G=
Transcript Alleles
HGVS
Amino-acid Change
NM_000769.4:c.636G=
MANE Select
NP_000760.1:p.Trp212=
ENST00000371321.9:c.636G=
MANE Select
ENSP00000360372.3:p.Trp212=
NM_000769.2:c.636G=
NP_000760.1:p.Trp212=
ENST00000371321.7:c.636G=
ENSP00000360372.3:p.Trp212=
ENST00000464755.1:c.1399G=
ENSP00000483243.1:n.1399G=
ENST00000645461.1:n.1689G=
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