Canonical Allele Identifier: CA2000559462
Gene: SDHD HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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