Canonical Allele Identifier: CA1239744308

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26283063T= , CM000664.2:g.26283063T=	GRCh38
NC_000002.11:g.26505931T= , CM000664.1:g.26505931T=	GRCh37
NC_000002.10:g.26359435T=	NCBI36
NG_007294.1:g.43111T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.1061+12T= MANE Select	ENSP00000325136.5:n.1061+12T=
ENST00000317799.9:c.1061+12T=	ENSP00000325136.5:n.1061+12T=
ENST00000405867.7:c.692+12T=	ENSP00000385411.3:n.692+12T=
ENST00000494615.1:n.2008+12T=
ENST00000537713.5:c.1016+12T=	ENSP00000444295.1:n.1016+12T=
ENST00000545822.2:c.995+12T=	ENSP00000442665.1:n.995+12T=
NM_000183.2:c.1061+12T=	NP_000174.1:n.1061+12T=
NM_001281512.1:c.1016+12T=	NP_001268441.1:n.1016+12T=
NM_001281513.1:c.995+12T=	NP_001268442.1:n.995+12T=
XM_011532803.1:c.1061+12T=	XP_011531105.1:n.1061+12T=
XM_011532804.1:c.995+12T=	XP_011531106.1:n.995+12T=
XM_024452830.1:c.1031+12T=	XP_024308598.1:n.1031+12T=
XM_024452831.1:c.995+12T=	XP_024308599.1:n.995+12T=
NM_000183.3:c.1061+12T= MANE Select	NP_000174.1:n.1061+12T=
NM_001281513.2:c.995+12T=	NP_001268442.1:n.995+12T=
NM_001281512.2:c.1016+12T=	NP_001268441.1:n.1016+12T=