Canonical Allele Identifier: CA364656519
Gene: ELOVL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.80631383G>C (hg19) chr6:g.79921666G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79921666G>C , CM000668.2:g.79921666G>C GRCh38
NC_000006.11:g.80631383G>C , CM000668.1:g.80631383G>C GRCh37
NC_000006.10:g.80688102G>C NCBI36
NG_009108.1:g.30933C>G
NG_009108.2:g.30933C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369816.5:c.500C>G MANE Select ENSP00000358831.4:p.Thr167Ser
ENST00000369816.4:c.500C>G ENSP00000358831.4:p.Thr167Ser
NM_022726.3:c.500C>G NP_073563.1:p.Thr167Ser
NM_022726.4:c.500C>G MANE Select NP_073563.1:p.Thr167Ser
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