Canonical Allele Identifier: CA224024385
Gene: OVOL1 HGNC NCBI

Linked Data

dbSNP Id: rs920152246
gnomAD v2: 11-65559302-T-A
gnomAD v3: 11-65791831-T-A
gnomAD v4: 11-65791831-T-A
MyVariant Identifiers: chr11:g.65559302T>A (hg19) chr11:g.65791831T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791831T>A , CM000673.2:g.65791831T>A GRCh38
NC_000011.9:g.65559302T>A , CM000673.1:g.65559302T>A GRCh37
NC_000011.8:g.65315878T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335987.8:c.101-2200T>A MANE Select ENSP00000337862.3:n.101-2200T>A
ENST00000335987.7:c.101-2200T>A ENSP00000337862.3:n.101-2200T>A
ENST00000531907.1:n.361-487T>A
NM_004561.3:c.101-2200T>A NP_004552.2:n.101-2200T>A
XM_005274018.3:c.-87+2138T>A XP_005274075.1:n.-87+2138T>A
XM_011545067.1:c.-86-2200T>A XP_011543369.1:n.-86-2200T>A
XM_011545068.1:c.-87+968T>A XP_011543370.1:n.-87+968T>A
XM_011545067.2:c.-86-2200T>A XP_011543369.1:n.-86-2200T>A
XM_011545068.3:c.-87+968T>A XP_011543370.1:n.-87+968T>A
XM_017017837.1:c.-86-2200T>A XP_016873326.1:n.-86-2200T>A
NM_004561.4:c.101-2200T>A MANE Select NP_004552.2:n.101-2200T>A
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