Canonical Allele Identifier: CA346096779

Gene: HADHB

Linked Data

• MyVariant Identifiers: chr2:g.26508335C>A (hg19) ; chr2:g.26285467C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26285467C>A , CM000664.2:g.26285467C>A	GRCh38
NC_000002.11:g.26508335C>A , CM000664.1:g.26508335C>A	GRCh37
NC_000002.10:g.26361839C>A	NCBI36
NG_007294.1:g.45515C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.1285C>A MANE Select	ENSP00000325136.5:p.Pro429Thr
ENST00000317799.9:c.1285C>A	ENSP00000325136.5:p.Pro429Thr
ENST00000405867.7:c.916C>A	ENSP00000385411.3:p.Pro306Thr
ENST00000494615.1:n.2232C>A
ENST00000537713.5:c.1240C>A	ENSP00000444295.1:p.Pro414Thr
ENST00000545822.2:c.1219C>A	ENSP00000442665.1:p.Pro407Thr
NM_000183.2:c.1285C>A	NP_000174.1:p.Pro429Thr
NM_001281512.1:c.1240C>A	NP_001268441.1:p.Pro414Thr
NM_001281513.1:c.1219C>A	NP_001268442.1:p.Pro407Thr
XM_011532803.1:c.1285C>A	XP_011531105.1:p.Pro429Thr
XM_011532804.1:c.1219C>A	XP_011531106.1:p.Pro407Thr
XM_024452830.1:c.1255C>A	XP_024308598.1:p.Pro419Thr
XM_024452831.1:c.1219C>A	XP_024308599.1:p.Pro407Thr
NM_000183.3:c.1285C>A MANE Select	NP_000174.1:p.Pro429Thr
NM_001281513.2:c.1219C>A	NP_001268442.1:p.Pro407Thr
NM_001281512.2:c.1240C>A	NP_001268441.1:p.Pro414Thr