Canonical Allele Identifier: CA2610265986
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94949098-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949098T>C , CM000672.2:g.94949098T>C GRCh38
NC_000010.10:g.96708855T>C , CM000672.1:g.96708855T>C GRCh37
NC_000010.9:g.96698845T>C NCBI36
NG_008385.1:g.15441T>C
NG_008385.2:g.15941T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.643-10T>C MANE Select ENSP00000260682.6:n.643-10T>C
ENST00000643112.1:c.643-10T>C ENSP00000496202.1:n.643-10T>C
ENST00000260682.6:c.643-10T>C ENSP00000260682.6:n.643-10T>C
ENST00000473496.1:n.414-10T>C
NM_000771.3:c.643-10T>C NP_000762.2:n.643-10T>C
NM_000771.4:c.643-10T>C MANE Select NP_000762.2:n.643-10T>C
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