Canonical Allele Identifier: CA2677321341
Gene: ELOVL2 HGNC NCBI

Linked Data

gnomAD v4: 6-10982132-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10982132A>T , CM000668.2:g.10982132A>T GRCh38
NC_000006.11:g.10982365A>T , CM000668.1:g.10982365A>T GRCh37
NC_000006.10:g.11090351A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000354666.4:c.*1649T>A MANE Select ENSP00000346693.3:n.*1649T>A
ENST00000354666.3:c.*1649T>A ENSP00000346693.3:n.*1649T>A
NM_017770.3:c.*1649T>A NP_060240.3:n.*1649T>A
XM_011514716.1:c.*1649T>A XP_011513018.1:n.*1649T>A
XM_011514717.1:c.*1649T>A XP_011513019.1:n.*1649T>A
XM_011514716.3:c.*1649T>A XP_011513018.1:n.*1649T>A
NM_017770.4:c.*1649T>A MANE Select NP_060240.3:n.*1649T>A
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