Canonical Allele Identifier: CA377672735
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94941913-T-C
MyVariant Identifiers: chr10:g.96701670T>C (hg19) chr10:g.94941913T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941913T>C , CM000672.2:g.94941913T>C GRCh38
NC_000010.10:g.96701670T>C , CM000672.1:g.96701670T>C GRCh37
NC_000010.9:g.96691660T>C NCBI36
NG_008385.1:g.8256T>C
NG_008385.2:g.8756T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.224T>C MANE Select ENSP00000260682.6:p.Val75Ala
ENST00000643112.1:c.224T>C ENSP00000496202.1:p.Val75Ala
ENST00000645207.1:n.377T>C
ENST00000260682.6:c.224T>C ENSP00000260682.6:p.Val75Ala
ENST00000461906.1:n.249T>C
NM_000771.3:c.224T>C NP_000762.2:p.Val75Ala
NM_000771.4:c.224T>C MANE Select NP_000762.2:p.Val75Ala
Search 100 bp 5'
Search 100 bp 3'