Canonical Allele Identifier: CA377670521
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540308C>G (hg19) chr10:g.94780551C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780551C>G , CM000672.2:g.94780551C>G GRCh38
NC_000010.10:g.96540308C>G , CM000672.1:g.96540308C>G GRCh37
NC_000010.9:g.96530298C>G NCBI36
NG_008384.2:g.22846C>G
NG_008384.3:g.22871C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.534C>G MANE Select ENSP00000360372.3:p.Ile178Met
ENST00000645461.1:n.1587C>G
ENST00000371321.7:c.534C>G ENSP00000360372.3:p.Ile178Met
ENST00000464755.1:c.1297C>G ENSP00000483243.1:n.1297C>G
NM_000769.2:c.534C>G NP_000760.1:p.Ile178Met
NM_000769.4:c.534C>G MANE Select NP_000760.1:p.Ile178Met
Search 100 bp 5'
Search 100 bp 3'