Canonical Allele Identifier: CA1979406101
Gene: OVOL1 HGNC NCBI

Linked Data

dbSNP Id: rs1858025143
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791849C>G , CM000673.2:g.65791849C>G GRCh38
NC_000011.9:g.65559320C>G , CM000673.1:g.65559320C>G GRCh37
NC_000011.8:g.65315896C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335987.8:c.101-2182C>G MANE Select ENSP00000337862.3:n.101-2182C>G
ENST00000335987.7:c.101-2182C>G ENSP00000337862.3:n.101-2182C>G
ENST00000531907.1:n.361-469C>G
NM_004561.3:c.101-2182C>G NP_004552.2:n.101-2182C>G
XM_005274018.3:c.-87+2156C>G XP_005274075.1:n.-87+2156C>G
XM_011545067.1:c.-86-2182C>G XP_011543369.1:n.-86-2182C>G
XM_011545068.1:c.-87+986C>G XP_011543370.1:n.-87+986C>G
XM_011545067.2:c.-86-2182C>G XP_011543369.1:n.-86-2182C>G
XM_011545068.3:c.-87+986C>G XP_011543370.1:n.-87+986C>G
XM_017017837.1:c.-86-2182C>G XP_016873326.1:n.-86-2182C>G
NM_004561.4:c.101-2182C>G MANE Select NP_004552.2:n.101-2182C>G
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