Canonical Allele Identifier: CA931385665
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032363107
gnomAD v3: 10-94988779-G-C
gnomAD v4: 10-94988779-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988779G>C , CM000672.2:g.94988779G>C GRCh38
NC_000010.10:g.96748536G>C , CM000672.1:g.96748536G>C GRCh37
NC_000010.9:g.96738526G>C NCBI36
NG_008385.1:g.55122G>C
NG_008385.2:g.55622G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-68G>C MANE Select ENSP00000260682.6:n.1292-68G>C
ENST00000643112.1:c.*301-68G>C ENSP00000496202.1:n.*301-68G>C
ENST00000260682.6:c.1292-68G>C ENSP00000260682.6:n.1292-68G>C
NM_000771.3:c.1292-68G>C NP_000762.2:n.1292-68G>C
NM_000771.4:c.1292-68G>C MANE Select NP_000762.2:n.1292-68G>C
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