Canonical Allele Identifier: CA2573805515
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849902G>T , CM000672.2:g.94849902G>T GRCh38
NC_000010.10:g.96609659G>T , CM000672.1:g.96609659G>T GRCh37
NC_000010.9:g.96599649G>T NCBI36
NG_008384.2:g.92197G>T
NG_008384.3:g.92222G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1150-15G>T MANE Select ENSP00000360372.3:n.1150-15G>T
ENST00000645461.1:n.2061-15G>T
ENST00000371321.7:c.1150-15G>T ENSP00000360372.3:n.1150-15G>T
ENST00000464755.1:c.1913-15G>T ENSP00000483243.1:n.1913-15G>T
NM_000769.2:c.1150-15G>T NP_000760.1:n.1150-15G>T
NM_000769.4:c.1150-15G>T MANE Select NP_000760.1:n.1150-15G>T