Canonical Allele Identifier: CA377670804
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1213978205
gnomAD v2: 10-96540396-G-T
gnomAD v3: 10-94780639-G-T
gnomAD v4: 10-94780639-G-T
MyVariant Identifiers: chr10:g.96540396G>T (hg19) chr10:g.94780639G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780639G>T , CM000672.2:g.94780639G>T GRCh38
NC_000010.10:g.96540396G>T , CM000672.1:g.96540396G>T GRCh37
NC_000010.9:g.96530386G>T NCBI36
NG_008384.2:g.22934G>T
NG_008384.3:g.22959G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.622G>T MANE Select ENSP00000360372.3:p.Val208Leu
ENST00000645461.1:n.1675G>T
ENST00000371321.7:c.622G>T ENSP00000360372.3:p.Val208Leu
ENST00000464755.1:c.1385G>T ENSP00000483243.1:n.1385G>T
NM_000769.2:c.622G>T NP_000760.1:p.Val208Leu
NM_000769.4:c.622G>T MANE Select NP_000760.1:p.Val208Leu
Search 100 bp 5'
Search 100 bp 3'