Canonical Allele Identifier: CA425202144

Gene: HADHB

Linked Data

• MyVariant Identifiers: chr2:g.26508373T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26285505T>G , CM000664.2:g.26285505T>G	GRCh38
NC_000002.11:g.26508373T>G , CM000664.1:g.26508373T>G	GRCh37
NC_000002.10:g.26361877T>G	NCBI36
NG_007294.1:g.45553T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.1323T>G MANE Select	ENSP00000325136.5:p.Ala441=
ENST00000317799.9:c.1323T>G	ENSP00000325136.5:p.Ala441=
ENST00000405867.7:c.954T>G	ENSP00000385411.3:p.Ala318=
ENST00000494615.1:n.2270T>G
ENST00000537713.5:c.1278T>G	ENSP00000444295.1:p.Ala426=
ENST00000545822.2:c.1257T>G	ENSP00000442665.1:p.Ala419=
NM_000183.2:c.1323T>G	NP_000174.1:p.Ala441=
NM_001281512.1:c.1278T>G	NP_001268441.1:p.Ala426=
NM_001281513.1:c.1257T>G	NP_001268442.1:p.Ala419=
XM_011532803.1:c.1323T>G	XP_011531105.1:p.Ala441=
XM_011532804.1:c.1257T>G	XP_011531106.1:p.Ala419=
XM_024452830.1:c.1293T>G	XP_024308598.1:p.Ala431=
XM_024452831.1:c.1257T>G	XP_024308599.1:p.Ala419=
NM_000183.3:c.1323T>G MANE Select	NP_000174.1:p.Ala441=
NM_001281513.2:c.1257T>G	NP_001268442.1:p.Ala419=
NM_001281512.2:c.1278T>G	NP_001268441.1:p.Ala426=