Canonical Allele Identifier: CA1929334662
Gene: CYP2C9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974395A= , CM000672.2:g.94974395A= GRCh38
NC_000010.10:g.96734152A= , CM000672.1:g.96734152A= GRCh37
NC_000010.9:g.96724142A= NCBI36
NG_008385.1:g.40738A=
NG_008385.2:g.41238A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2150A= MANE Select ENSP00000260682.6:n.961+2150A=
ENST00000643112.1:c.820-6788A= ENSP00000496202.1:n.820-6788A=
ENST00000260682.6:c.961+2150A= ENSP00000260682.6:n.961+2150A=
NM_000771.3:c.961+2150A= NP_000762.2:n.961+2150A=
NM_000771.4:c.961+2150A= MANE Select NP_000762.2:n.961+2150A=
Search 100 bp 5'
Search 100 bp 3'