Canonical Allele Identifier: CA377671348
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96541665A>C (hg19) chr10:g.94781908A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781908A>C , CM000672.2:g.94781908A>C GRCh38
NC_000010.10:g.96541665A>C , CM000672.1:g.96541665A>C GRCh37
NC_000010.9:g.96531655A>C NCBI36
NG_008384.2:g.24203A>C
NG_008384.3:g.24228A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.730A>C MANE Select ENSP00000360372.3:p.Ile244Leu
ENST00000645461.1:n.1783A>C
ENST00000371321.7:c.730A>C ENSP00000360372.3:p.Ile244Leu
ENST00000464755.1:c.1493A>C ENSP00000483243.1:n.1493A>C
NM_000769.2:c.730A>C NP_000760.1:p.Ile244Leu
NM_000769.4:c.730A>C MANE Select NP_000760.1:p.Ile244Leu
Search 100 bp 5'
Search 100 bp 3'