Canonical Allele Identifier: CA1929222272
Gene: CYP2C19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781780A= , CM000672.2:g.94781780A= GRCh38
NC_000010.10:g.96541537A= , CM000672.1:g.96541537A= GRCh37
NC_000010.9:g.96531527A= NCBI36
NG_008384.2:g.24075A=
NG_008384.3:g.24100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.643-41A= MANE Select ENSP00000360372.3:n.643-41A=
ENST00000645461.1:n.1696-41A=
ENST00000371321.7:c.643-41A= ENSP00000360372.3:n.643-41A=
ENST00000464755.1:c.1406-41A= ENSP00000483243.1:n.1406-41A=
NM_000769.2:c.643-41A= NP_000760.1:n.643-41A=
NM_000769.4:c.643-41A= MANE Select NP_000760.1:n.643-41A=
Search 100 bp 5'
Search 100 bp 3'