Canonical Allele Identifier: CA211676329
Gene: CYP2C19 HGNC NCBI
MTND4P19 HGNC NCBI

Linked Data

dbSNP Id: rs937009766
MyVariant Identifiers: chr10:g.96534270T>G (hg19) chr10:g.94774513T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94774513T>G , CM000672.2:g.94774513T>G GRCh38
NC_000010.10:g.96534270T>G , CM000672.1:g.96534270T>G GRCh37
NC_000010.9:g.96524260T>G NCBI36
NG_008384.2:g.16808T>G
NG_008384.3:g.16833T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.169-545T>G (CYP2C19) MANE Select ENSP00000360372.3:n.169-545T>G
ENST00000645461.1:n.677T>G (CYP2C19)
ENST00000371321.7:c.169-545T>G (CYP2C19) ENSP00000360372.3:n.169-545T>G
ENST00000446659.1:n.121A>C (MTND4P19)
ENST00000464755.1:c.932-545T>G ENSP00000483243.1:n.932-545T>G
ENST00000480405.2:c.169-545T>G (CYP2C19) ENSP00000483847.1:n.169-545T>G
NM_000769.2:c.169-545T>G (CYP2C19) NP_000760.1:n.169-545T>G
NM_000769.4:c.169-545T>G (CYP2C19) MANE Select NP_000760.1:n.169-545T>G
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