Canonical Allele Identifier: CA377674036
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96708905G>C (hg19) chr10:g.94949148G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949148G>C , CM000672.2:g.94949148G>C GRCh38
NC_000010.10:g.96708905G>C , CM000672.1:g.96708905G>C GRCh37
NC_000010.9:g.96698895G>C NCBI36
NG_008385.1:g.15491G>C
NG_008385.2:g.15991G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.683G>C MANE Select ENSP00000260682.6:p.Gly228Ala
ENST00000643112.1:c.683G>C ENSP00000496202.1:p.Gly228Ala
ENST00000260682.6:c.683G>C ENSP00000260682.6:p.Gly228Ala
ENST00000473496.1:n.454G>C
NM_000771.3:c.683G>C NP_000762.2:p.Gly228Ala
NM_000771.4:c.683G>C MANE Select NP_000762.2:p.Gly228Ala
Search 100 bp 5'
Search 100 bp 3'