Canonical Allele Identifier: CA2610265007
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94849816-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849816C>G , CM000672.2:g.94849816C>G GRCh38
NC_000010.10:g.96609573C>G , CM000672.1:g.96609573C>G GRCh37
NC_000010.9:g.96599563C>G NCBI36
NG_008384.2:g.92111C>G
NG_008384.3:g.92136C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1150-101C>G MANE Select ENSP00000360372.3:n.1150-101C>G
ENST00000645461.1:n.2061-101C>G
ENST00000371321.7:c.1150-101C>G ENSP00000360372.3:n.1150-101C>G
ENST00000464755.1:c.1913-101C>G ENSP00000483243.1:n.1913-101C>G
NM_000769.2:c.1150-101C>G NP_000760.1:n.1150-101C>G
NM_000769.4:c.1150-101C>G MANE Select NP_000760.1:n.1150-101C>G
Search 100 bp 5'
Search 100 bp 3'