Canonical Allele Identifier: CA1929218952
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775742G= , CM000672.2:g.94775742G= GRCh38
NC_000010.10:g.96535499G= , CM000672.1:g.96535499G= GRCh37
NC_000010.9:g.96525489G= NCBI36
NG_008384.2:g.18037G=
NG_008384.3:g.18062G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+203G= MANE Select ENSP00000360372.3:n.481+203G=
ENST00000645461.1:n.1534+203G=
ENST00000371321.7:c.481+203G= ENSP00000360372.3:n.481+203G=
ENST00000464755.1:c.1244+203G= ENSP00000483243.1:n.1244+203G=
ENST00000480405.2:c.*195G= ENSP00000483847.1:n.*195G=
NM_000769.2:c.481+203G= NP_000760.1:n.481+203G=
NM_000769.4:c.481+203G= MANE Select NP_000760.1:n.481+203G=
Search 100 bp 5'
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