Canonical Allele Identifier: CA2610265131
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94852582-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852582A>C , CM000672.2:g.94852582A>C GRCh38
NC_000010.10:g.96612339A>C , CM000672.1:g.96612339A>C GRCh37
NC_000010.9:g.96602329A>C NCBI36
NG_008384.2:g.94877A>C
NG_008384.3:g.94902A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-151A>C MANE Select ENSP00000360372.3:n.1292-151A>C
ENST00000645461.1:n.2203-151A>C
ENST00000371321.7:c.1292-151A>C ENSP00000360372.3:n.1292-151A>C
ENST00000464755.1:c.2055-151A>C ENSP00000483243.1:n.2055-151A>C
NM_000769.2:c.1292-151A>C NP_000760.1:n.1292-151A>C
NM_000769.4:c.1292-151A>C MANE Select NP_000760.1:n.1292-151A>C
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