Canonical Allele Identifier: CA377670008
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1469529559
MyVariant Identifiers: chr10:g.96535203A>G (hg19) chr10:g.94775446A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775446A>G , CM000672.2:g.94775446A>G GRCh38
NC_000010.10:g.96535203A>G , CM000672.1:g.96535203A>G GRCh37
NC_000010.9:g.96525193A>G NCBI36
NG_008384.2:g.17741A>G
NG_008384.3:g.17766A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.388A>G MANE Select ENSP00000360372.3:p.Thr130Ala
ENST00000645461.1:n.1441A>G
ENST00000371321.7:c.388A>G ENSP00000360372.3:p.Thr130Ala
ENST00000464755.1:c.1151A>G ENSP00000483243.1:n.1151A>G
ENST00000480405.2:c.388A>G ENSP00000483847.1:p.Thr130Ala
NM_000769.2:c.388A>G NP_000760.1:p.Thr130Ala
NM_000769.4:c.388A>G MANE Select NP_000760.1:p.Thr130Ala
Search 100 bp 5'
Search 100 bp 3'