Canonical Allele Identifier: CA470829752
Gene: CYP2C19 HGNC NCBI
MTND4P19 HGNC NCBI

Linked Data

gnomAD v4: 10-94774508-G-T
MyVariant Identifiers: chr10:g.96534265G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94774508G>T , CM000672.2:g.94774508G>T GRCh38
NC_000010.10:g.96534265G>T , CM000672.1:g.96534265G>T GRCh37
NC_000010.9:g.96524255G>T NCBI36
NG_008384.2:g.16803G>T
NG_008384.3:g.16828G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.169-550G>T (CYP2C19) MANE Select ENSP00000360372.3:n.169-550G>T
ENST00000645461.1:n.672G>T (CYP2C19)
ENST00000371321.7:c.169-550G>T (CYP2C19) ENSP00000360372.3:n.169-550G>T
ENST00000446659.1:n.126C>A (MTND4P19)
ENST00000464755.1:c.932-550G>T ENSP00000483243.1:n.932-550G>T
ENST00000480405.2:c.169-550G>T (CYP2C19) ENSP00000483847.1:n.169-550G>T
NM_000769.2:c.169-550G>T (CYP2C19) NP_000760.1:n.169-550G>T
NM_000769.4:c.169-550G>T (CYP2C19) MANE Select NP_000760.1:n.169-550G>T
Search 100 bp 5'
Search 100 bp 3'