Canonical Allele Identifier: CA1929278451
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1849632831
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850252A>C , CM000672.2:g.94850252A>C GRCh38
NC_000010.10:g.96610009A>C , CM000672.1:g.96610009A>C GRCh37
NC_000010.9:g.96599999A>C NCBI36
NG_008384.2:g.92547A>C
NG_008384.3:g.92572A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1291+194A>C MANE Select ENSP00000360372.3:n.1291+194A>C
ENST00000645461.1:n.2202+194A>C
ENST00000371321.7:c.1291+194A>C ENSP00000360372.3:n.1291+194A>C
ENST00000464755.1:c.2054+194A>C ENSP00000483243.1:n.2054+194A>C
NM_000769.2:c.1291+194A>C NP_000760.1:n.1291+194A>C
NM_000769.4:c.1291+194A>C MANE Select NP_000760.1:n.1291+194A>C
Search 100 bp 5'
Search 100 bp 3'