Canonical Allele Identifier: CA2643679617

Gene: SDHB

Linked Data

• gnomAD v4: 1-17044680-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044682_17044684del , CM000663.2:g.17044682_17044684del	GRCh38
NC_000001.10:g.17371177_17371179del , CM000663.1:g.17371177_17371179del	GRCh37
NC_000001.9:g.17243764_17243766del	NCBI36
NG_012340.1:g.14488_14490del , LRG_316:g.14488_14490del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.29+78_29+80del	ENSP00000481376.2:n.29+78_29+80del
ENST00000491274.6:c.158+78_158+80del	ENSP00000480482.2:n.158+78_158+80del
ENST00000375499.8:c.200+78_200+80del MANE Select	ENSP00000364649.3:n.200+78_200+80del
ENST00000375499.7:c.200+78_200+80del	ENSP00000364649.3:n.200+78_200+80del
ENST00000463045.2:c.29+78_29+80del	ENSP00000481376.1:n.29+78_29+80del
ENST00000466613.2:n.212+78_212+80del
ENST00000475506.1:n.117+78_117+80del
ENST00000485515.5:n.188+78_188+80del
ENST00000491274.5:c.158+78_158+80del	ENSP00000480482.1:n.158+78_158+80del
NM_003000.2:c.200+78_200+80del , LRG_316t1:c.200+78_200+80del	NP_002991.2:n.200+78_200+80del
NM_003000.3:c.200+78_200+80del MANE Select	NP_002991.2:n.200+78_200+80del