Canonical Allele Identifier: CA938947967
Gene: OVOL1 HGNC NCBI

Linked Data

dbSNP Id: rs1858023669

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791799A>G , CM000673.2:g.65791799A>G GRCh38
NC_000011.9:g.65559270A>G , CM000673.1:g.65559270A>G GRCh37
NC_000011.8:g.65315846A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335987.8:c.101-2232A>G MANE Select ENSP00000337862.3:n.101-2232A>G
ENST00000335987.7:c.101-2232A>G ENSP00000337862.3:n.101-2232A>G
ENST00000531907.1:n.361-519A>G
NM_004561.3:c.101-2232A>G NP_004552.2:n.101-2232A>G
XM_005274018.3:c.-87+2106A>G XP_005274075.1:n.-87+2106A>G
XM_011545067.1:c.-86-2232A>G XP_011543369.1:n.-86-2232A>G
XM_011545068.1:c.-87+936A>G XP_011543370.1:n.-87+936A>G
XM_011545067.2:c.-86-2232A>G XP_011543369.1:n.-86-2232A>G
XM_011545068.3:c.-87+936A>G XP_011543370.1:n.-87+936A>G
XM_017017837.1:c.-86-2232A>G XP_016873326.1:n.-86-2232A>G
NM_004561.4:c.101-2232A>G MANE Select NP_004552.2:n.101-2232A>G