Canonical Allele Identifier: CA2610264766
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94781676-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781676C>T , CM000672.2:g.94781676C>T GRCh38
NC_000010.10:g.96541433C>T , CM000672.1:g.96541433C>T GRCh37
NC_000010.9:g.96531423C>T NCBI36
NG_008384.2:g.23971C>T
NG_008384.3:g.23996C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.643-145C>T MANE Select ENSP00000360372.3:n.643-145C>T
ENST00000645461.1:n.1696-145C>T
ENST00000371321.7:c.643-145C>T ENSP00000360372.3:n.643-145C>T
ENST00000464755.1:c.1406-145C>T ENSP00000483243.1:n.1406-145C>T
NM_000769.2:c.643-145C>T NP_000760.1:n.643-145C>T
NM_000769.4:c.643-145C>T MANE Select NP_000760.1:n.643-145C>T
Search 100 bp 5'
Search 100 bp 3'