Canonical Allele Identifier: CA52252337
Gene: SUCLG1 HGNC NCBI

Linked Data

dbSNP Id: rs966836601
gnomAD v3: 2-84425732-A-C
gnomAD v4: 2-84425732-A-C
MyVariant Identifiers: chr2:g.84652856A>C (hg19) chr2:g.84425732A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84425732A>C , CM000664.2:g.84425732A>C GRCh38
NC_000002.11:g.84652856A>C , CM000664.1:g.84652856A>C GRCh37
NC_000002.10:g.84506367A>C NCBI36
NG_016755.1:g.38731T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393868.7:c.826-129T>G MANE Select ENSP00000377446.2:n.826-129T>G
ENST00000651342.1:c.*266-129T>G ENSP00000498471.1:n.*266-129T>G
ENST00000393868.6:c.826-129T>G ENSP00000377446.2:n.826-129T>G
ENST00000484365.1:n.1205T>G
ENST00000487809.1:n.573-129T>G
ENST00000491123.5:n.672-129T>G
NM_003849.3:c.826-129T>G NP_003840.2:n.826-129T>G
NM_003849.4:c.826-129T>G MANE Select NP_003840.2:n.826-129T>G
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