Canonical Allele Identifier: CA595638688
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1177209031
gnomAD v2: 10-96609657-A-G
gnomAD v4: 10-94849900-A-G
MyVariant Identifiers: chr10:g.96609657A>G (hg19) chr10:g.94849900A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849900A>G , CM000672.2:g.94849900A>G GRCh38
NC_000010.10:g.96609657A>G , CM000672.1:g.96609657A>G GRCh37
NC_000010.9:g.96599647A>G NCBI36
NG_008384.2:g.92195A>G
NG_008384.3:g.92220A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1150-17A>G MANE Select ENSP00000360372.3:n.1150-17A>G
ENST00000645461.1:n.2061-17A>G
ENST00000371321.7:c.1150-17A>G ENSP00000360372.3:n.1150-17A>G
ENST00000464755.1:c.1913-17A>G ENSP00000483243.1:n.1913-17A>G
NM_000769.2:c.1150-17A>G NP_000760.1:n.1150-17A>G
NM_000769.4:c.1150-17A>G MANE Select NP_000760.1:n.1150-17A>G
Search 100 bp 5'
Search 100 bp 3'