Canonical Allele Identifier: CA1929278262
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849958_94849959delinsCA , CM000672.2:g.94849958_94849959delinsCA GRCh38
NC_000010.10:g.96609715_96609716delinsCA , CM000672.1:g.96609715_96609716delinsCA GRCh37
NC_000010.9:g.96599705_96599706delinsCA NCBI36
NG_008384.2:g.92253_92254delinsCA
NG_008384.3:g.92278_92279delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1191_1192delinsCA MANE Select ENSP00000360372.3:p.Asp397=
ENST00000645461.1:n.2102_2103delinsCA
ENST00000371321.7:c.1191_1192delinsCA ENSP00000360372.3:p.Asp397=
ENST00000464755.1:c.1954_1955delinsCA ENSP00000483243.1:n.1954_1955delinsCA
NM_000769.2:c.1191_1192delinsCA NP_000760.1:p.Asp397=
NM_000769.4:c.1191_1192delinsCA MANE Select NP_000760.1:p.Asp397=
Search 100 bp 5'
Search 100 bp 3'