Canonical Allele Identifier: CA1929218896
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775626A= , CM000672.2:g.94775626A= GRCh38
NC_000010.10:g.96535383A= , CM000672.1:g.96535383A= GRCh37
NC_000010.9:g.96525373A= NCBI36
NG_008384.2:g.17921A=
NG_008384.3:g.17946A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+87A= MANE Select ENSP00000360372.3:n.481+87A=
ENST00000645461.1:n.1534+87A=
ENST00000371321.7:c.481+87A= ENSP00000360372.3:n.481+87A=
ENST00000464755.1:c.1244+87A= ENSP00000483243.1:n.1244+87A=
ENST00000480405.2:c.*79A= ENSP00000483847.1:n.*79A=
NM_000769.2:c.481+87A= NP_000760.1:n.481+87A=
NM_000769.4:c.481+87A= MANE Select NP_000760.1:n.481+87A=
Search 100 bp 5'
Search 100 bp 3'