Canonical Allele Identifier: CA5616274
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs28399504

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762706A>T , CM000672.2:g.94762706A>T GRCh38
NC_000010.10:g.96522463A>T , CM000672.1:g.96522463A>T GRCh37
NC_000010.9:g.96512453A>T NCBI36
NG_008384.2:g.5001A>T
NG_008384.3:g.5026A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1A>T MANE Select ENSP00000360372.3:p.Met1Leu
ENST00000371321.7:c.1A>T ENSP00000360372.3:p.Met1Leu
ENST00000464755.1:n.932-12352A>T ENSP00000483243.1:n.932-12352A>T
ENST00000480405.2:c.1A>T ENSP00000483847.1:p.Met1Leu
NM_000769.2:c.1A>T NP_000760.1:p.Met1Leu
NM_000769.4:c.1A>T MANE Select NP_000760.1:p.Met1Leu