Canonical Allele Identifier: CA211699989
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs569438544
gnomAD v2: 10-96708524-CGTGAATGTA-C
gnomAD v3: 10-94948767-CGTGAATGTA-C
gnomAD v4: 10-94948767-CGTGAATGTA-C
MyVariant Identifiers: chr10:g.96708525_96708533del (hg19) chr10:g.94948768_94948776del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94948770_94948778del , CM000672.2:g.94948770_94948778del GRCh38
NC_000010.10:g.96708527_96708535del , CM000672.1:g.96708527_96708535del GRCh37
NC_000010.9:g.96698517_96698525del NCBI36
NG_008385.1:g.15113_15121del
NG_008385.2:g.15613_15621del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-338_643-330del MANE Select ENSP00000260682.6:n.643-338_643-330del
ENST00000643112.1:c.643-338_643-330del ENSP00000496202.1:n.643-338_643-330del
ENST00000260682.6:c.643-338_643-330del ENSP00000260682.6:n.643-338_643-330del
ENST00000473496.1:n.414-338_414-330del
NM_000771.3:c.643-338_643-330del NP_000762.2:n.643-338_643-330del
NM_000771.4:c.643-338_643-330del MANE Select NP_000762.2:n.643-338_643-330del
Search 100 bp 5'
Search 100 bp 3'