Canonical Allele Identifier: CA2610264130
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94775773-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775773C>T , CM000672.2:g.94775773C>T GRCh38
NC_000010.10:g.96535530C>T , CM000672.1:g.96535530C>T GRCh37
NC_000010.9:g.96525520C>T NCBI36
NG_008384.2:g.18068C>T
NG_008384.3:g.18093C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+234C>T MANE Select ENSP00000360372.3:n.481+234C>T
ENST00000645461.1:n.1534+234C>T
ENST00000371321.7:c.481+234C>T ENSP00000360372.3:n.481+234C>T
ENST00000464755.1:c.1244+234C>T ENSP00000483243.1:n.1244+234C>T
ENST00000480405.2:c.*226C>T ENSP00000483847.1:n.*226C>T
NM_000769.2:c.481+234C>T NP_000760.1:n.481+234C>T
NM_000769.4:c.481+234C>T MANE Select NP_000760.1:n.481+234C>T
Search 100 bp 5'
Search 100 bp 3'