Canonical Allele Identifier: CA2574620198
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94941758-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941762del , CM000672.2:g.94941762del GRCh38
NC_000010.10:g.96701519del , CM000672.1:g.96701519del GRCh37
NC_000010.9:g.96691509del NCBI36
NG_008385.1:g.8105del
NG_008385.2:g.8605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-96del MANE Select ENSP00000260682.6:n.169-96del
ENST00000643112.1:c.169-96del ENSP00000496202.1:n.169-96del
ENST00000645207.1:n.226del
ENST00000260682.6:c.169-96del ENSP00000260682.6:n.169-96del
ENST00000461906.1:n.194-96del
NM_000771.3:c.169-96del NP_000762.2:n.169-96del
NM_000771.4:c.169-96del MANE Select NP_000762.2:n.169-96del
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Search 100 bp 3'