Canonical Allele Identifier: CA2610264626
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94780702-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780702T>C , CM000672.2:g.94780702T>C GRCh38
NC_000010.10:g.96540459T>C , CM000672.1:g.96540459T>C GRCh37
NC_000010.9:g.96530449T>C NCBI36
NG_008384.2:g.22997T>C
NG_008384.3:g.23022T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+43T>C MANE Select ENSP00000360372.3:n.642+43T>C
ENST00000645461.1:n.1695+43T>C
ENST00000371321.7:c.642+43T>C ENSP00000360372.3:n.642+43T>C
ENST00000464755.1:c.1405+43T>C ENSP00000483243.1:n.1405+43T>C
NM_000769.2:c.642+43T>C NP_000760.1:n.642+43T>C
NM_000769.4:c.642+43T>C MANE Select NP_000760.1:n.642+43T>C
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