Canonical Allele Identifier: CA224024381
Gene: OVOL1 HGNC NCBI

Linked Data

dbSNP Id: rs562815026

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791826C>T , CM000673.2:g.65791826C>T GRCh38
NC_000011.9:g.65559297C>T , CM000673.1:g.65559297C>T GRCh37
NC_000011.8:g.65315873C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335987.8:c.101-2205C>T MANE Select ENSP00000337862.3:n.101-2205C>T
ENST00000335987.7:c.101-2205C>T ENSP00000337862.3:n.101-2205C>T
ENST00000531907.1:n.361-492C>T
NM_004561.3:c.101-2205C>T NP_004552.2:n.101-2205C>T
XM_005274018.3:c.-87+2133C>T XP_005274075.1:n.-87+2133C>T
XM_011545067.1:c.-86-2205C>T XP_011543369.1:n.-86-2205C>T
XM_011545068.1:c.-87+963C>T XP_011543370.1:n.-87+963C>T
XM_011545067.2:c.-86-2205C>T XP_011543369.1:n.-86-2205C>T
XM_011545068.3:c.-87+963C>T XP_011543370.1:n.-87+963C>T
XM_017017837.1:c.-86-2205C>T XP_016873326.1:n.-86-2205C>T
NM_004561.4:c.101-2205C>T MANE Select NP_004552.2:n.101-2205C>T