Canonical Allele Identifier: CA1929271576
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94842767_94842768delinsAC , CM000672.2:g.94842767_94842768delinsAC GRCh38
NC_000010.10:g.96602524_96602525delinsAC , CM000672.1:g.96602524_96602525delinsAC GRCh37
NC_000010.9:g.96592514_96592515delinsAC NCBI36
NG_008384.2:g.85062_85063delinsAC
NG_008384.3:g.85087_85088delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.962-70_962-69delinsAC MANE Select ENSP00000360372.3:n.962-70_962-69delinsAC...
ENST00000645461.1:n.1873-70_1873-69delinsAC
ENST00000371321.7:c.962-70_962-69delinsAC ENSP00000360372.3:n.962-70_962-69delinsAC...
ENST00000464755.1:c.1725-70_1725-69delinsAC ENSP00000483243.1:n.1725-70_1725-69delins...
NM_000769.2:c.962-70_962-69delinsAC NP_000760.1:n.962-70_962-69delinsAC
NM_000769.4:c.962-70_962-69delinsAC MANE Select NP_000760.1:n.962-70_962-69delinsAC