Canonical Allele Identifier: CA427118655
Gene: SUCLG1 HGNC NCBI

Linked Data

gnomAD v4: 2-84425466-T-C
MyVariant Identifiers: chr2:g.84652590T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84425466T>C , CM000664.2:g.84425466T>C GRCh38
NC_000002.11:g.84652590T>C , CM000664.1:g.84652590T>C GRCh37
NC_000002.10:g.84506101T>C NCBI36
NG_016755.1:g.38997A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393868.7:c.963A>G MANE Select ENSP00000377446.2:p.Ala321=
ENST00000651342.1:c.*403A>G ENSP00000498471.1:n.*403A>G
ENST00000393868.6:c.963A>G ENSP00000377446.2:p.Ala321=
ENST00000484365.1:n.1471A>G
ENST00000487809.1:n.710A>G
ENST00000491123.5:n.809A>G
NM_003849.3:c.963A>G NP_003840.2:p.Ala321=
NM_003849.4:c.963A>G MANE Select NP_003840.2:p.Ala321=