Canonical Allele Identifier: CA134135498
Gene: ELOVL2 HGNC NCBI

Linked Data

dbSNP Id: rs755910510
gnomAD v4: 6-10982140-G-T
MyVariant Identifiers: chr6:g.10982373G>T (hg19) chr6:g.10982140G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10982140G>T , CM000668.2:g.10982140G>T GRCh38
NC_000006.11:g.10982373G>T , CM000668.1:g.10982373G>T GRCh37
NC_000006.10:g.11090359G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000354666.4:c.*1641C>A MANE Select ENSP00000346693.3:n.*1641C>A
ENST00000354666.3:c.*1641C>A ENSP00000346693.3:n.*1641C>A
NM_017770.3:c.*1641C>A NP_060240.3:n.*1641C>A
XM_011514716.1:c.*1641C>A XP_011513018.1:n.*1641C>A
XM_011514717.1:c.*1641C>A XP_011513019.1:n.*1641C>A
XM_011514716.3:c.*1641C>A XP_011513018.1:n.*1641C>A
NM_017770.4:c.*1641C>A MANE Select NP_060240.3:n.*1641C>A
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