Canonical Allele Identifier: CA2000559491
Gene: SDHD HGNC NCBI

Linked Data

dbSNP Id: rs1865615275

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086843G>A , CM000673.2:g.112086843G>A GRCh38
NC_000011.9:g.111957567G>A , CM000673.1:g.111957567G>A GRCh37
NC_000011.8:g.111462777G>A NCBI36
NG_012337.2:g.4997G>A
NG_033145.1:g.4956C>T
NG_012337.3:g.4997G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000640554.1:c.-65G>A ENSP00000491141.1:n.-65G>A
ENST00000375549.7:c.-65G>A ENSP00000364699.3:n.-65G>A
ENST00000614349.4:c.-65G>A ENSP00000480666.1:n.-65G>A
NM_001276503.1:c.-65G>A NP_001263432.1:n.-65G>A
NM_001276504.1:c.-65G>A NP_001263433.1:n.-65G>A
NM_001276506.1:c.-65G>A NP_001263435.1:n.-65G>A
NM_003002.3:c.-65G>A NP_002993.1:n.-65G>A
NR_077060.1:n.20G>A