Canonical Allele Identifier: CA2610265021

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94849844-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94849844G>T , CM000672.2:g.94849844G>T	GRCh38
NC_000010.10:g.96609601G>T , CM000672.1:g.96609601G>T	GRCh37
NC_000010.9:g.96599591G>T	NCBI36
NG_008384.2:g.92139G>T
NG_008384.3:g.92164G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1150-73G>T MANE Select	ENSP00000360372.3:n.1150-73G>T
ENST00000645461.1:n.2061-73G>T
ENST00000371321.7:c.1150-73G>T	ENSP00000360372.3:n.1150-73G>T
ENST00000464755.1:c.1913-73G>T	ENSP00000483243.1:n.1913-73G>T
NM_000769.2:c.1150-73G>T	NP_000760.1:n.1150-73G>T
NM_000769.4:c.1150-73G>T MANE Select	NP_000760.1:n.1150-73G>T