Canonical Allele Identifier: CA425204431

Gene: HADHB

Linked Data

• MyVariant Identifiers: chr2:g.26486258C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26263390C>G , CM000664.2:g.26263390C>G	GRCh38
NC_000002.11:g.26486258C>G , CM000664.1:g.26486258C>G	GRCh37
NC_000002.10:g.26339762C>G	NCBI36
NG_007294.1:g.23438C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.120C>G MANE Select	ENSP00000325136.5:p.Thr40=
ENST00000317799.9:c.120C>G	ENSP00000325136.5:p.Thr40=
ENST00000405867.7:c.120C>G	ENSP00000385411.3:p.Thr40=
ENST00000412805.5:c.120C>G	ENSP00000413103.1:p.Thr40=
ENST00000425035.5:c.120C>G	ENSP00000404633.1:p.Thr40=
ENST00000448743.5:c.120C>G	ENSP00000415300.1:p.Thr40=
ENST00000494615.1:n.1067C>G
ENST00000537713.5:c.120C>G	ENSP00000444295.1:p.Thr40=
ENST00000545822.2:c.54C>G	ENSP00000442665.1:p.Thr18=
NM_000183.2:c.120C>G	NP_000174.1:p.Thr40=
NM_001281512.1:c.120C>G	NP_001268441.1:p.Thr40=
NM_001281513.1:c.54C>G	NP_001268442.1:p.Thr18=
XM_011532803.1:c.120C>G	XP_011531105.1:p.Thr40=
XM_011532804.1:c.54C>G	XP_011531106.1:p.Thr18=
XM_024452830.1:c.90C>G	XP_024308598.1:p.Thr30=
XM_024452831.1:c.54C>G	XP_024308599.1:p.Thr18=
NM_000183.3:c.120C>G MANE Select	NP_000174.1:p.Thr40=
NM_001281513.2:c.54C>G	NP_001268442.1:p.Thr18=
NM_001281512.2:c.120C>G	NP_001268441.1:p.Thr40=