Canonical Allele Identifier: CA377675172
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96609782A>T (hg19) chr10:g.94850025A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850025A>T , CM000672.2:g.94850025A>T GRCh38
NC_000010.10:g.96609782A>T , CM000672.1:g.96609782A>T GRCh37
NC_000010.9:g.96599772A>T NCBI36
NG_008384.2:g.92320A>T
NG_008384.3:g.92345A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1258A>T MANE Select ENSP00000360372.3:p.Lys420Ter
ENST00000645461.1:n.2169A>T
ENST00000371321.7:c.1258A>T ENSP00000360372.3:p.Lys420Ter
ENST00000464755.1:c.2021A>T ENSP00000483243.1:n.2021A>T
NM_000769.2:c.1258A>T NP_000760.1:p.Lys420Ter
NM_000769.4:c.1258A>T MANE Select NP_000760.1:p.Lys420Ter
Search 100 bp 5'
Search 100 bp 3'