Canonical Allele Identifier: CA5617255
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs761679167
ExAC: 10:96740897 C / G
gnomAD v2: 10-96740897-C-G
gnomAD v4: 10-94981140-C-G
MyVariant Identifiers: chr10:g.96740897C>G (hg19) chr10:g.94981140C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981140C>G , CM000672.2:g.94981140C>G GRCh38
NC_000010.10:g.96740897C>G , CM000672.1:g.96740897C>G GRCh37
NC_000010.9:g.96730887C>G NCBI36
NG_008385.1:g.47483C>G
NG_008385.2:g.47983C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-43C>G MANE Select ENSP00000260682.6:n.962-43C>G
ENST00000643112.1:c.820-43C>G ENSP00000496202.1:n.820-43C>G
ENST00000260682.6:c.962-43C>G ENSP00000260682.6:n.962-43C>G
NM_000771.3:c.962-43C>G NP_000762.2:n.962-43C>G
NM_000771.4:c.962-43C>G MANE Select NP_000762.2:n.962-43C>G
Search 100 bp 5'
Search 100 bp 3'