Canonical Allele Identifier: CA653585454
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762632T>G , CM000672.2:g.94762632T>G GRCh38
NC_000010.10:g.96522389T>G , CM000672.1:g.96522389T>G GRCh37
NC_000010.9:g.96512379T>G NCBI36
NG_008384.2:g.4927T>G
NG_008384.3:g.4952T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-74T>G ENSP00000360372.3:n.-74T>G
ENST00000464755.1:c.932-12426T>G ENSP00000483243.1:n.932-12426T>G