Canonical Allele Identifier: CA2610265062
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94850127-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850127A>C , CM000672.2:g.94850127A>C GRCh38
NC_000010.10:g.96609884A>C , CM000672.1:g.96609884A>C GRCh37
NC_000010.9:g.96599874A>C NCBI36
NG_008384.2:g.92422A>C
NG_008384.3:g.92447A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1291+69A>C MANE Select ENSP00000360372.3:n.1291+69A>C
ENST00000645461.1:n.2202+69A>C
ENST00000371321.7:c.1291+69A>C ENSP00000360372.3:n.1291+69A>C
ENST00000464755.1:c.2054+69A>C ENSP00000483243.1:n.2054+69A>C
NM_000769.2:c.1291+69A>C NP_000760.1:n.1291+69A>C
NM_000769.4:c.1291+69A>C MANE Select NP_000760.1:n.1291+69A>C
Search 100 bp 5'
Search 100 bp 3'