Canonical Allele Identifier: CA670165692
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1391069996
MyVariant Identifiers: chr10:g.96541984C>A (hg19) chr10:g.94782227C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782227C>A , CM000672.2:g.94782227C>A GRCh38
NC_000010.10:g.96541984C>A , CM000672.1:g.96541984C>A GRCh37
NC_000010.9:g.96531974C>A NCBI36
NG_008384.2:g.24522C>A
NG_008384.3:g.24547C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+230C>A MANE Select ENSP00000360372.3:n.819+230C>A
ENST00000645461.1:n.1872+230C>A
ENST00000371321.7:c.819+230C>A ENSP00000360372.3:n.819+230C>A
ENST00000464755.1:c.1582+230C>A ENSP00000483243.1:n.1582+230C>A
NM_000769.2:c.819+230C>A NP_000760.1:n.819+230C>A
NM_000769.4:c.819+230C>A MANE Select NP_000760.1:n.819+230C>A
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