Canonical Allele Identifier: CA1610232040
Gene: ELOVL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10982029C= , CM000668.2:g.10982029C= GRCh38
NC_000006.11:g.10982262C= , CM000668.1:g.10982262C= GRCh37
NC_000006.10:g.11090248C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000354666.4:c.*1752G= MANE Select ENSP00000346693.3:n.*1752G=
ENST00000354666.3:c.*1752G= ENSP00000346693.3:n.*1752G=
NM_017770.3:c.*1752G= NP_060240.3:n.*1752G=
XM_011514716.1:c.*1752G= XP_011513018.1:n.*1752G=
XM_011514717.1:c.*1752G= XP_011513019.1:n.*1752G=
XM_011514716.3:c.*1752G= XP_011513018.1:n.*1752G=
NM_017770.4:c.*1752G= MANE Select NP_060240.3:n.*1752G=
Search 100 bp 5'
Search 100 bp 3'