Canonical Allele Identifier: CA2793910
Community Standard Title: NM_000283.4(PDE6B):c.316C>T (p.Leu106=)
Gene: PDE6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.625942C>T , CM000666.2:g.625942C>T GRCh38
NC_000004.11:g.619731C>T , CM000666.1:g.619731C>T GRCh37
NC_000004.10:g.609731C>T NCBI36
NG_009839.1:g.5369C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000283.4:c.316C>T MANE Select NP_000274.3:p.Leu106=
ENST00000496514.6:c.316C>T MANE Select ENSP00000420295.1:p.Leu106=
NM_000283.3:c.316C>T NP_000274.2:p.Leu106=
NM_001145291.1:c.316C>T NP_001138763.1:p.Leu106=
NM_001145291.2:c.316C>T NP_001138763.2:p.Leu106=
ENST00000255622.10:c.316C>T ENSP00000255622.6:p.Leu106=
ENST00000496514.5:c.316C>T ENSP00000420295.1:p.Leu106=
XM_011513473.1:c.535C>T XP_011511775.1:p.Leu179=
XM_011513473.3:c.535C>T XP_011511775.1:p.Leu179=
XM_011513474.1:c.535C>T XP_011511776.1:p.Leu179=
XM_011513474.3:c.535C>T XP_011511776.1:p.Leu179=
XM_011513475.1:c.316C>T XP_011511777.1:p.Leu106=
XM_011513475.2:c.316C>T XP_011511777.1:p.Leu106=
XM_011513476.1:c.535C>T XP_011511778.1:p.Leu179=
XM_011513476.3:c.535C>T XP_011511778.1:p.Leu179=