Canonical Allele Identifier: CA2648776677

Gene: SDHC

Linked Data

• gnomAD v4: 1-161362747-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161362747G>T , CM000663.2:g.161362747G>T	GRCh38
NC_000001.10:g.161332537G>T , CM000663.1:g.161332537G>T	GRCh37
NC_000001.9:g.159599161G>T	NCBI36
NG_012767.1:g.53372G>T , LRG_317:g.53372G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*825G>T	ENSP00000482902.2:n.*825G>T
ENST00000367975.7:c.*314G>T MANE Select	ENSP00000356953.3:n.*314G>T
ENST00000342751.8:c.*207G>T	ENSP00000356952.3:n.*207G>T
ENST00000367975.6:c.*314G>T	ENSP00000356953.2:n.*314G>T
NM_001035511.1:c.*207G>T	NP_001030588.1:n.*207G>T
NM_001035512.1:c.*314G>T	NP_001030589.1:n.*314G>T
NM_001035513.1:c.*314G>T	NP_001030590.1:n.*314G>T
NM_001278172.1:c.*207G>T	NP_001265101.1:n.*207G>T
NM_003001.3:c.*314G>T , LRG_317t1:c.*314G>T	NP_002992.1:n.*314G>T
NR_103459.1:n.881G>T
NM_001035511.2:c.*207G>T	NP_001030588.1:n.*207G>T
NM_001035512.2:c.*314G>T	NP_001030589.1:n.*314G>T
NM_001035513.2:c.*314G>T	NP_001030590.1:n.*314G>T
NM_001278172.2:c.*207G>T	NP_001265101.1:n.*207G>T
NM_003001.5:c.*314G>T MANE Select	NP_002992.1:n.*314G>T
NR_103459.2:n.876G>T