Canonical Allele Identifier: CA377673941
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96708865A>C (hg19) chr10:g.94949108A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949108A>C , CM000672.2:g.94949108A>C GRCh38
NC_000010.10:g.96708865A>C , CM000672.1:g.96708865A>C GRCh37
NC_000010.9:g.96698855A>C NCBI36
NG_008385.1:g.15451A>C
NG_008385.2:g.15951A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.643A>C MANE Select ENSP00000260682.6:p.Ile215Leu
ENST00000643112.1:c.643A>C ENSP00000496202.1:p.Ile215Leu
ENST00000260682.6:c.643A>C ENSP00000260682.6:p.Ile215Leu
ENST00000473496.1:n.414A>C
NM_000771.3:c.643A>C NP_000762.2:p.Ile215Leu
NM_000771.4:c.643A>C MANE Select NP_000762.2:p.Ile215Leu
Search 100 bp 5'
Search 100 bp 3'