Canonical Allele Identifier: CA2610265035

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94849897-CCTATGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94849900_94849905del , CM000672.2:g.94849900_94849905del	GRCh38
NC_000010.10:g.96609657_96609662del , CM000672.1:g.96609657_96609662del	GRCh37
NC_000010.9:g.96599647_96599652del	NCBI36
NG_008384.2:g.92195_92200del
NG_008384.3:g.92220_92225del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1150-17_1150-12del MANE Select	ENSP00000360372.3:n.1150-17_1150-12del
ENST00000645461.1:n.2061-17_2061-12del
ENST00000371321.7:c.1150-17_1150-12del	ENSP00000360372.3:n.1150-17_1150-12del
ENST00000464755.1:c.1913-17_1913-12del	ENSP00000483243.1:n.1913-17_1913-12del
NM_000769.2:c.1150-17_1150-12del	NP_000760.1:n.1150-17_1150-12del
NM_000769.4:c.1150-17_1150-12del MANE Select	NP_000760.1:n.1150-17_1150-12del