Canonical Allele Identifier: CA1560517

Gene: HADHB

Linked Data

• ClinVar Variation Id: 894830
• ClinVar RCV Id: RCV001136587
• dbSNP Id: rs781574694
• ExAC: 2:26508386 C / T
• gnomAD v2: 2-26508386-C-T
• gnomAD v3: 2-26285518-C-T
• gnomAD v4: 2-26285518-C-T
• MyVariant Identifiers: chr2:g.26508386C>T (hg19) ; chr2:g.26285518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26285518C>T , CM000664.2:g.26285518C>T	GRCh38
NC_000002.11:g.26508386C>T , CM000664.1:g.26508386C>T	GRCh37
NC_000002.10:g.26361890C>T	NCBI36
NG_007294.1:g.45566C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317799.10:c.1336C>T MANE Select	ENSP00000325136.5:p.Arg446Trp
ENST00000317799.9:c.1336C>T	ENSP00000325136.5:p.Arg446Trp
ENST00000405867.7:c.967C>T	ENSP00000385411.3:p.Arg323Trp
ENST00000494615.1:n.2283C>T
ENST00000537713.5:c.1291C>T	ENSP00000444295.1:p.Arg431Trp
ENST00000545822.2:c.1270C>T	ENSP00000442665.1:p.Arg424Trp
NM_000183.2:c.1336C>T	NP_000174.1:p.Arg446Trp
NM_001281512.1:c.1291C>T	NP_001268441.1:p.Arg431Trp
NM_001281513.1:c.1270C>T	NP_001268442.1:p.Arg424Trp
XM_011532803.1:c.1336C>T	XP_011531105.1:p.Arg446Trp
XM_011532804.1:c.1270C>T	XP_011531106.1:p.Arg424Trp
XM_024452830.1:c.1306C>T	XP_024308598.1:p.Arg436Trp
XM_024452831.1:c.1270C>T	XP_024308599.1:p.Arg424Trp
NM_000183.3:c.1336C>T MANE Select	NP_000174.1:p.Arg446Trp
NM_001281513.2:c.1270C>T	NP_001268442.1:p.Arg424Trp
NM_001281512.2:c.1291C>T	NP_001268441.1:p.Arg431Trp