Canonical Allele Identifier: CA364656528
Gene: ELOVL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.80631386A>T (hg19) chr6:g.79921669A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79921669A>T , CM000668.2:g.79921669A>T GRCh38
NC_000006.11:g.80631386A>T , CM000668.1:g.80631386A>T GRCh37
NC_000006.10:g.80688105A>T NCBI36
NG_009108.1:g.30930T>A
NG_009108.2:g.30930T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369816.5:c.497T>A MANE Select ENSP00000358831.4:p.Phe166Tyr
ENST00000369816.4:c.497T>A ENSP00000358831.4:p.Phe166Tyr
NM_022726.3:c.497T>A NP_073563.1:p.Phe166Tyr
NM_022726.4:c.497T>A MANE Select NP_073563.1:p.Phe166Tyr
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