Canonical Allele Identifier: CA338227766
Community Standard Title: NM_003000.3(SDHB):c.183T>A (p.Tyr61Ter)
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044778A>T , CM000663.2:g.17044778A>T GRCh38
NC_000001.10:g.17371273A>T , CM000663.1:g.17371273A>T GRCh37
NC_000001.9:g.17243860A>T NCBI36
NG_012340.1:g.14393T>A , LRG_316:g.14393T>A

Transcript Alleles

HGVS Amino-acid Change
NM_003000.3:c.183T>A MANE Select NP_002991.2:p.Tyr61Ter
ENST00000375499.8:c.183T>A MANE Select ENSP00000364649.3:p.Tyr61Ter
NM_003000.2:c.183T>A , LRG_316t1:c.183T>A NP_002991.2:p.Tyr61Ter
ENST00000375499.7:c.183T>A ENSP00000364649.3:p.Tyr61Ter
ENST00000463045.2:c.12T>A ENSP00000481376.1:p.Tyr4Ter
ENST00000463045.3:c.12T>A ENSP00000481376.2:p.Tyr4Ter
ENST00000466613.2:n.195T>A
ENST00000475506.1:n.100T>A
ENST00000485515.5:n.171T>A
ENST00000491274.5:c.141T>A ENSP00000480482.1:p.Tyr47Ter
ENST00000491274.6:c.141T>A ENSP00000480482.2:p.Tyr47Ter