Canonical Allele Identifier: CA1610232201
Gene: ELOVL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10982235T= , CM000668.2:g.10982235T= GRCh38
NC_000006.11:g.10982468T= , CM000668.1:g.10982468T= GRCh37
NC_000006.10:g.11090454T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354666.4:c.*1546A= MANE Select ENSP00000346693.3:n.*1546A=
ENST00000354666.3:c.*1546A= ENSP00000346693.3:n.*1546A=
NM_017770.3:c.*1546A= NP_060240.3:n.*1546A=
XM_011514716.1:c.*1546A= XP_011513018.1:n.*1546A=
XM_011514717.1:c.*1546A= XP_011513019.1:n.*1546A=
XM_011514716.3:c.*1546A= XP_011513018.1:n.*1546A=
NM_017770.4:c.*1546A= MANE Select NP_060240.3:n.*1546A=
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