Canonical Allele Identifier: CA1239744199

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26282983C= , CM000664.2:g.26282983C=	GRCh38
NC_000002.11:g.26505851C= , CM000664.1:g.26505851C=	GRCh37
NC_000002.10:g.26359355C=	NCBI36
NG_007294.1:g.43031C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.1014-21C= MANE Select	ENSP00000325136.5:n.1014-21C=
ENST00000317799.9:c.1014-21C=	ENSP00000325136.5:n.1014-21C=
ENST00000405867.7:c.645-21C=	ENSP00000385411.3:n.645-21C=
ENST00000494615.1:n.1961-21C=
ENST00000537713.5:c.969-21C=	ENSP00000444295.1:n.969-21C=
ENST00000545822.2:c.948-21C=	ENSP00000442665.1:n.948-21C=
NM_000183.2:c.1014-21C=	NP_000174.1:n.1014-21C=
NM_001281512.1:c.969-21C=	NP_001268441.1:n.969-21C=
NM_001281513.1:c.948-21C=	NP_001268442.1:n.948-21C=
XM_011532803.1:c.1014-21C=	XP_011531105.1:n.1014-21C=
XM_011532804.1:c.948-21C=	XP_011531106.1:n.948-21C=
XM_024452830.1:c.984-21C=	XP_024308598.1:n.984-21C=
XM_024452831.1:c.948-21C=	XP_024308599.1:n.948-21C=
NM_000183.3:c.1014-21C= MANE Select	NP_000174.1:n.1014-21C=
NM_001281513.2:c.948-21C=	NP_001268442.1:n.948-21C=
NM_001281512.2:c.969-21C=	NP_001268441.1:n.969-21C=