Canonical Allele Identifier: CA2648776079
Gene: SDHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161340457G>A , CM000663.2:g.161340457G>A GRCh38
NC_000001.10:g.161310247G>A , CM000663.1:g.161310247G>A GRCh37
NC_000001.9:g.159576871G>A NCBI36
NG_012767.1:g.31082G>A , LRG_317:g.31082G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.*181-137G>A ENSP00000482902.2:n.*181-137G>A
ENST00000367975.7:c.180-137G>A MANE Select ENSP00000356953.3:n.180-137G>A
ENST00000342751.8:c.180-137G>A ENSP00000356952.3:n.180-137G>A
ENST00000367975.6:c.180-137G>A ENSP00000356953.2:n.180-137G>A
ENST00000392169.6:c.21-137G>A ENSP00000376009.2:n.21-137G>A
ENST00000432287.6:c.78-137G>A ENSP00000390558.2:n.78-137G>A
ENST00000470743.4:c.278-137G>A
ENST00000504963.5:c.*3-137G>A ENSP00000423929.1:n.*3-137G>A
ENST00000513009.5:c.78-137G>A ENSP00000423260.1:n.78-137G>A
NM_001035511.1:c.180-137G>A NP_001030588.1:n.180-137G>A
NM_001035512.1:c.78-137G>A NP_001030589.1:n.78-137G>A
NM_001035513.1:c.21-137G>A NP_001030590.1:n.21-137G>A
NM_001278172.1:c.78-137G>A NP_001265101.1:n.78-137G>A
NM_003001.3:c.180-137G>A , LRG_317t1:c.180-137G>A NP_002992.1:n.180-137G>A
NR_103459.1:n.237-137G>A
NM_001035511.2:c.180-137G>A NP_001030588.1:n.180-137G>A
NM_001035512.2:c.78-137G>A NP_001030589.1:n.78-137G>A
NM_001035513.2:c.21-137G>A NP_001030590.1:n.21-137G>A
NM_001278172.2:c.78-137G>A NP_001265101.1:n.78-137G>A
NM_003001.5:c.180-137G>A MANE Select NP_002992.1:n.180-137G>A
NR_103459.2:n.232-137G>A