Canonical Allele Identifier: CA346092971

Gene: HADHB

Linked Data

• MyVariant Identifiers: chr2:g.26502072T>G (hg19) ; chr2:g.26279204T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26279204T>G , CM000664.2:g.26279204T>G	GRCh38
NC_000002.11:g.26502072T>G , CM000664.1:g.26502072T>G	GRCh37
NC_000002.10:g.26355576T>G	NCBI36
NG_007294.1:g.39252T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317799.10:c.700T>G MANE Select	ENSP00000325136.5:p.Phe234Val
ENST00000317799.9:c.700T>G	ENSP00000325136.5:p.Phe234Val
ENST00000405867.7:c.443-790T>G	ENSP00000385411.3:n.443-790T>G
ENST00000494615.1:n.1647T>G
ENST00000537713.5:c.655T>G	ENSP00000444295.1:p.Phe219Val
ENST00000545822.2:c.634T>G	ENSP00000442665.1:p.Phe212Val
NM_000183.2:c.700T>G	NP_000174.1:p.Phe234Val
NM_001281512.1:c.655T>G	NP_001268441.1:p.Phe219Val
NM_001281513.1:c.634T>G	NP_001268442.1:p.Phe212Val
XM_011532803.1:c.700T>G	XP_011531105.1:p.Phe234Val
XM_011532804.1:c.634T>G	XP_011531106.1:p.Phe212Val
XM_024452830.1:c.670T>G	XP_024308598.1:p.Phe224Val
XM_024452831.1:c.634T>G	XP_024308599.1:p.Phe212Val
NM_000183.3:c.700T>G MANE Select	NP_000174.1:p.Phe234Val
NM_001281513.2:c.634T>G	NP_001268442.1:p.Phe212Val
NM_001281512.2:c.655T>G	NP_001268441.1:p.Phe219Val