Canonical Allele Identifier: CA595322218
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs914248804
gnomAD v2: 10-96540470-G-C
gnomAD v3: 10-94780713-G-C
gnomAD v4: 10-94780713-G-C
MyVariant Identifiers: chr10:g.96540470G>C (hg19) chr10:g.94780713G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780713G>C , CM000672.2:g.94780713G>C GRCh38
NC_000010.10:g.96540470G>C , CM000672.1:g.96540470G>C GRCh37
NC_000010.9:g.96530460G>C NCBI36
NG_008384.2:g.23008G>C
NG_008384.3:g.23033G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+54G>C MANE Select ENSP00000360372.3:n.642+54G>C
ENST00000645461.1:n.1695+54G>C
ENST00000371321.7:c.642+54G>C ENSP00000360372.3:n.642+54G>C
ENST00000464755.1:c.1405+54G>C ENSP00000483243.1:n.1405+54G>C
NM_000769.2:c.642+54G>C NP_000760.1:n.642+54G>C
NM_000769.4:c.642+54G>C MANE Select NP_000760.1:n.642+54G>C
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