Canonical Allele Identifier: CA2610262462
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762659del , CM000672.2:g.94762659del GRCh38
NC_000010.10:g.96522416del , CM000672.1:g.96522416del GRCh37
NC_000010.9:g.96512406del NCBI36
NG_008384.2:g.4954del
NG_008384.3:g.4979del

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-47del ENSP00000360372.3:n.-47del
ENST00000464755.1:c.932-12399del ENSP00000483243.1:n.932-12399del