Canonical Allele Identifier: CA211680795
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1029871700
MyVariant Identifiers: chr10:g.94780402T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780402T>G , CM000672.2:g.94780402T>G GRCh38
NC_000010.10:g.96540159T>G , CM000672.1:g.96540159T>G GRCh37
NC_000010.9:g.96530149T>G NCBI36
NG_008384.2:g.22697T>G
NG_008384.3:g.22722T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-97T>G MANE Select ENSP00000360372.3:n.482-97T>G
ENST00000645461.1:n.1535-97T>G
ENST00000371321.7:c.482-97T>G ENSP00000360372.3:n.482-97T>G
ENST00000464755.1:c.1245-97T>G ENSP00000483243.1:n.1245-97T>G
NM_000769.2:c.482-97T>G NP_000760.1:n.482-97T>G
NM_000769.4:c.482-97T>G MANE Select NP_000760.1:n.482-97T>G