Canonical Allele Identifier: CA2610264949

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94782141-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94782143del , CM000672.2:g.94782143del	GRCh38
NC_000010.10:g.96541900del , CM000672.1:g.96541900del	GRCh37
NC_000010.9:g.96531890del	NCBI36
NG_008384.2:g.24438del
NG_008384.3:g.24463del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.819+146del MANE Select	ENSP00000360372.3:n.819+146del
ENST00000645461.1:n.1872+146del
ENST00000371321.7:c.819+146del	ENSP00000360372.3:n.819+146del
ENST00000464755.1:c.1582+146del	ENSP00000483243.1:n.1582+146del
NM_000769.2:c.819+146del	NP_000760.1:n.819+146del
NM_000769.4:c.819+146del MANE Select	NP_000760.1:n.819+146del