Canonical Allele Identifier: CA2000559465

Gene: SDHD

Linked Data

• dbSNP Id: rs544421571
• gnomAD v4: 11-112086826-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086826T>G , CM000673.2:g.112086826T>G	GRCh38
NC_000011.9:g.111957550T>G , CM000673.1:g.111957550T>G	GRCh37
NC_000011.8:g.111462760T>G	NCBI36
NG_012337.2:g.4980T>G
NG_033145.1:g.4973A>C
NG_012337.3:g.4980T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000640554.1:c.-82T>G	ENSP00000491141.1:n.-82T>G
ENST00000375549.7:c.-82T>G	ENSP00000364699.3:n.-82T>G
ENST00000614349.4:c.-82T>G	ENSP00000480666.1:n.-82T>G
NM_001276503.1:c.-82T>G	NP_001263432.1:n.-82T>G
NM_001276504.1:c.-82T>G	NP_001263433.1:n.-82T>G
NM_001276506.1:c.-82T>G	NP_001263435.1:n.-82T>G
NM_003002.3:c.-82T>G	NP_002993.1:n.-82T>G
NR_077060.1:n.3T>G