Canonical Allele Identifier: CA595638651
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs769966695
gnomAD v2: 10-96541545-C-A
gnomAD v4: 10-94781788-C-A
COSMIC: COSN24303362 COSN24303363 COSN24303364 COSN24303365
MyVariant Identifiers: chr10:g.96541545C>A (hg19) chr10:g.94781788C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781788C>A , CM000672.2:g.94781788C>A GRCh38
NC_000010.10:g.96541545C>A , CM000672.1:g.96541545C>A GRCh37
NC_000010.9:g.96531535C>A NCBI36
NG_008384.2:g.24083C>A
NG_008384.3:g.24108C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.643-33C>A MANE Select ENSP00000360372.3:n.643-33C>A
ENST00000645461.1:n.1696-33C>A
ENST00000371321.7:c.643-33C>A ENSP00000360372.3:n.643-33C>A
ENST00000464755.1:c.1406-33C>A ENSP00000483243.1:n.1406-33C>A
NM_000769.2:c.643-33C>A NP_000760.1:n.643-33C>A
NM_000769.4:c.643-33C>A MANE Select NP_000760.1:n.643-33C>A
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