Canonical Allele Identifier: CA2610264621
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94780698-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780698A>C , CM000672.2:g.94780698A>C GRCh38
NC_000010.10:g.96540455A>C , CM000672.1:g.96540455A>C GRCh37
NC_000010.9:g.96530445A>C NCBI36
NG_008384.2:g.22993A>C
NG_008384.3:g.23018A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+39A>C MANE Select ENSP00000360372.3:n.642+39A>C
ENST00000645461.1:n.1695+39A>C
ENST00000371321.7:c.642+39A>C ENSP00000360372.3:n.642+39A>C
ENST00000464755.1:c.1405+39A>C ENSP00000483243.1:n.1405+39A>C
NM_000769.2:c.642+39A>C NP_000760.1:n.642+39A>C
NM_000769.4:c.642+39A>C MANE Select NP_000760.1:n.642+39A>C
Search 100 bp 5'
Search 100 bp 3'