Canonical Allele Identifier: CA5616529
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs566311971
ExAC: 10:96541595 C / A
gnomAD v2: 10-96541595-C-A
gnomAD v3: 10-94781838-C-A
gnomAD v4: 10-94781838-C-A
MyVariant Identifiers: chr10:g.96541595C>A (hg19) chr10:g.94781838C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781838C>A , CM000672.2:g.94781838C>A GRCh38
NC_000010.10:g.96541595C>A , CM000672.1:g.96541595C>A GRCh37
NC_000010.9:g.96531585C>A NCBI36
NG_008384.2:g.24133C>A
NG_008384.3:g.24158C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.660C>A MANE Select ENSP00000360372.3:p.Pro220=
ENST00000645461.1:n.1713C>A
ENST00000371321.7:c.660C>A ENSP00000360372.3:p.Pro220=
ENST00000464755.1:c.1423C>A ENSP00000483243.1:n.1423C>A
NM_000769.2:c.660C>A NP_000760.1:p.Pro220=
NM_000769.4:c.660C>A MANE Select NP_000760.1:p.Pro220=
Search 100 bp 5'
Search 100 bp 3'