Canonical Allele Identifier: CA470832306
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1262244551
gnomAD v2: 10-96541754-G-A
gnomAD v3: 10-94781997-G-A
gnomAD v4: 10-94781997-G-A
MyVariant Identifiers: chr10:g.96541754G>A (hg19) chr10:g.94781997G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781997G>A , CM000672.2:g.94781997G>A GRCh38
NC_000010.10:g.96541754G>A , CM000672.1:g.96541754G>A GRCh37
NC_000010.9:g.96531744G>A NCBI36
NG_008384.2:g.24292G>A
NG_008384.3:g.24317G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819G>A MANE Select ENSP00000360372.3:p.Lys273=
ENST00000645461.1:n.1872G>A
ENST00000371321.7:c.819G>A ENSP00000360372.3:p.Lys273=
ENST00000464755.1:c.1582G>A ENSP00000483243.1:n.1582G>A
NM_000769.2:c.819G>A NP_000760.1:p.Lys273=
NM_000769.4:c.819G>A MANE Select NP_000760.1:p.Lys273=
Search 100 bp 5'
Search 100 bp 3'