Canonical Allele Identifier: CA1929218241
Gene: CYP2C19 HGNC NCBI
MTND4P19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94774451T= , CM000672.2:g.94774451T= GRCh38
NC_000010.10:g.96534208T= , CM000672.1:g.96534208T= GRCh37
NC_000010.9:g.96524198T= NCBI36
NG_008384.2:g.16746T=
NG_008384.3:g.16771T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.169-607T= (CYP2C19) MANE Select ENSP00000360372.3:n.169-607T=
ENST00000645461.1:n.615T= (CYP2C19)
ENST00000371321.7:c.169-607T= (CYP2C19) ENSP00000360372.3:n.169-607T=
ENST00000446659.1:n.183A= (MTND4P19)
ENST00000464755.1:c.932-607T= ENSP00000483243.1:n.932-607T=
ENST00000480405.2:c.169-607T= (CYP2C19) ENSP00000483847.1:n.169-607T=
NM_000769.2:c.169-607T= (CYP2C19) NP_000760.1:n.169-607T=
NM_000769.4:c.169-607T= (CYP2C19) MANE Select NP_000760.1:n.169-607T=
Search 100 bp 5'
Search 100 bp 3'