Canonical Allele Identifier: CA364656526
Gene: ELOVL4 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000369816.5:c.497T>G MANE Select ENSP00000358831.4:p.Phe166Cys
ENST00000369816.4:c.497T>G ENSP00000358831.4:p.Phe166Cys
NM_022726.3:c.497T>G NP_073563.1:p.Phe166Cys
NM_022726.4:c.497T>G MANE Select NP_073563.1:p.Phe166Cys
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