Canonical Allele Identifier: CA2610266449
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94981122-TTGCTAC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981123_94981128del , CM000672.2:g.94981123_94981128del GRCh38
NC_000010.10:g.96740880_96740885del , CM000672.1:g.96740880_96740885del GRCh37
NC_000010.9:g.96730870_96730875del NCBI36
NG_008385.1:g.47466_47471del
NG_008385.2:g.47966_47971del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.962-60_962-55del MANE Select ENSP00000260682.6:n.962-60_962-55del
ENST00000643112.1:c.820-60_820-55del ENSP00000496202.1:n.820-60_820-55del
ENST00000260682.6:c.962-60_962-55del ENSP00000260682.6:n.962-60_962-55del
NM_000771.3:c.962-60_962-55del NP_000762.2:n.962-60_962-55del
NM_000771.4:c.962-60_962-55del MANE Select NP_000762.2:n.962-60_962-55del
Search 100 bp 5'
Search 100 bp 3'