Canonical Allele Identifier: CA446596413
Community Standard Title: NM_016604.4(KDM3B):c.423G>A (p.Leu141=)
Gene: KDM3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138375155G>A , CM000667.2:g.138375155G>A GRCh38
NC_000005.9:g.137710844G>A , CM000667.1:g.137710844G>A GRCh37
NC_000005.8:g.137738743G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_016604.4:c.423G>A MANE Select NP_057688.3:p.Leu141=
ENST00000314358.10:c.423G>A MANE Select ENSP00000326563.5:p.Leu141=
NM_016604.3:c.423G>A NP_057688.2:p.Leu141=
ENST00000314358.9:c.423G>A ENSP00000326563.5:p.Leu141=
ENST00000510866.5:c.231G>A ENSP00000425186.1:p.Leu77=
ENST00000512928.1:n.112G>A
XM_005272018.3:c.423G>A XP_005272075.1:p.Leu141=
XM_005272018.4:c.423G>A XP_005272075.1:p.Leu141=
XM_011543488.1:c.291G>A XP_011541790.1:p.Leu97=
XM_011543488.2:c.291G>A XP_011541790.1:p.Leu97=
XM_011543489.1:c.279G>A XP_011541791.1:p.Leu93=
XM_011543489.2:c.279G>A XP_011541791.1:p.Leu93=
XM_024446115.1:c.-52G>A XP_024301883.1:n.-52G>A