Canonical Allele Identifier: CA346096874

Gene: HADHB

Linked Data

• MyVariant Identifiers: chr2:g.26508381G>T (hg19) ; chr2:g.26285513G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26285513G>T , CM000664.2:g.26285513G>T	GRCh38
NC_000002.11:g.26508381G>T , CM000664.1:g.26508381G>T	GRCh37
NC_000002.10:g.26361885G>T	NCBI36
NG_007294.1:g.45561G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317799.10:c.1331G>T MANE Select	ENSP00000325136.5:p.Arg444Ile
ENST00000317799.9:c.1331G>T	ENSP00000325136.5:p.Arg444Ile
ENST00000405867.7:c.962G>T	ENSP00000385411.3:p.Arg321Ile
ENST00000494615.1:n.2278G>T
ENST00000537713.5:c.1286G>T	ENSP00000444295.1:p.Arg429Ile
ENST00000545822.2:c.1265G>T	ENSP00000442665.1:p.Arg422Ile
NM_000183.2:c.1331G>T	NP_000174.1:p.Arg444Ile
NM_001281512.1:c.1286G>T	NP_001268441.1:p.Arg429Ile
NM_001281513.1:c.1265G>T	NP_001268442.1:p.Arg422Ile
XM_011532803.1:c.1331G>T	XP_011531105.1:p.Arg444Ile
XM_011532804.1:c.1265G>T	XP_011531106.1:p.Arg422Ile
XM_024452830.1:c.1301G>T	XP_024308598.1:p.Arg434Ile
XM_024452831.1:c.1265G>T	XP_024308599.1:p.Arg422Ile
NM_000183.3:c.1331G>T MANE Select	NP_000174.1:p.Arg444Ile
NM_001281513.2:c.1265G>T	NP_001268442.1:p.Arg422Ile
NM_001281512.2:c.1286G>T	NP_001268441.1:p.Arg429Ile