Canonical Allele Identifier: CA2581539829
Gene: ELOVL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10982126G>C , CM000668.2:g.10982126G>C GRCh38
NC_000006.11:g.10982359G>C , CM000668.1:g.10982359G>C GRCh37
NC_000006.10:g.11090345G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000354666.4:c.*1655C>G MANE Select ENSP00000346693.3:n.*1655C>G
ENST00000354666.3:c.*1655C>G ENSP00000346693.3:n.*1655C>G
NM_017770.3:c.*1655C>G NP_060240.3:n.*1655C>G
XM_011514716.1:c.*1655C>G XP_011513018.1:n.*1655C>G
XM_011514717.1:c.*1655C>G XP_011513019.1:n.*1655C>G
XM_011514716.3:c.*1655C>G XP_011513018.1:n.*1655C>G
NM_017770.4:c.*1655C>G MANE Select NP_060240.3:n.*1655C>G