Canonical Allele Identifier: CA2610264589
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94842776_94842783dup , CM000672.2:g.94842776_94842783dup GRCh38
NC_000010.10:g.96602533_96602540dup , CM000672.1:g.96602533_96602540dup GRCh37
NC_000010.9:g.96592523_96592530dup NCBI36
NG_008384.2:g.85071_85078dup
NG_008384.3:g.85096_85103dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.962-61_962-54dup MANE Select ENSP00000360372.3:n.962-61_962-54dup
ENST00000645461.1:n.1873-61_1873-54dup
ENST00000371321.7:c.962-61_962-54dup ENSP00000360372.3:n.962-61_962-54dup
ENST00000464755.1:c.1725-61_1725-54dup ENSP00000483243.1:n.1725-61_1725-54dup
NM_000769.2:c.962-61_962-54dup NP_000760.1:n.962-61_962-54dup
NM_000769.4:c.962-61_962-54dup MANE Select NP_000760.1:n.962-61_962-54dup