Canonical Allele Identifier: CA915943645

Gene: SDHC

Linked Data

• ClinVar Variation Id: 646979
• ClinVar RCV Id: RCV000801370 ; RCV003472367
• dbSNP Id: rs1571851753

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328500A>C , CM000663.2:g.161328500A>C	GRCh38
NC_000001.10:g.161298290A>C , CM000663.1:g.161298290A>C	GRCh37
NC_000001.9:g.159564914A>C	NCBI36
NG_012767.1:g.19125A>C , LRG_317:g.19125A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*180+3A>C	ENSP00000482902.2:n.*180+3A>C
ENST00000367975.7:c.179+3A>C MANE Select	ENSP00000356953.3:n.179+3A>C
ENST00000342751.8:c.179+3A>C	ENSP00000356952.3:n.179+3A>C
ENST00000367975.6:c.179+3A>C	ENSP00000356953.2:n.179+3A>C
ENST00000392169.6:c.21-12094A>C	ENSP00000376009.2:n.21-12094A>C
ENST00000432287.6:c.77+4830A>C	ENSP00000390558.2:n.77+4830A>C
ENST00000470743.4:c.277+3A>C
ENST00000504963.5:c.179+3A>C	ENSP00000423929.1:n.179+3A>C
ENST00000513009.5:c.77+4830A>C	ENSP00000423260.1:n.77+4830A>C
NM_001035511.1:c.179+3A>C	NP_001030588.1:n.179+3A>C
NM_001035512.1:c.77+4830A>C	NP_001030589.1:n.77+4830A>C
NM_001035513.1:c.21-12094A>C	NP_001030590.1:n.21-12094A>C
NM_001278172.1:c.77+4830A>C	NP_001265101.1:n.77+4830A>C
NM_003001.3:c.179+3A>C , LRG_317t1:c.179+3A>C	NP_002992.1:n.179+3A>C
NR_103459.1:n.209+3A>C
NM_001035511.2:c.179+3A>C	NP_001030588.1:n.179+3A>C
NM_001035512.2:c.77+4830A>C	NP_001030589.1:n.77+4830A>C
NM_001035513.2:c.21-12094A>C	NP_001030590.1:n.21-12094A>C
NM_001278172.2:c.77+4830A>C	NP_001265101.1:n.77+4830A>C
NM_003001.5:c.179+3A>C MANE Select	NP_002992.1:n.179+3A>C
NR_103459.2:n.204+3A>C