Canonical Allele Identifier: CA378824494
Gene: ECHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1849142571
gnomAD v4: 10-133373288-T-A
MyVariant Identifiers: chr10:g.135186792T>A (hg19) chr10:g.133373288T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373288T>A , CM000672.2:g.133373288T>A GRCh38
NC_000010.10:g.135186792T>A , CM000672.1:g.135186792T>A GRCh37
NC_000010.9:g.135036782T>A NCBI36
NG_042077.1:g.5117A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.46A>T MANE Select ENSP00000357535.3:p.Arg16Trp
ENST00000368547.3:c.46A>T ENSP00000357535.3:p.Arg16Trp
NM_004092.3:c.46A>T NP_004083.3:p.Arg16Trp
XR_002956965.1:n.109A>T
NM_004092.4:c.46A>T MANE Select NP_004083.3:p.Arg16Trp
Search 100 bp 5'
Search 100 bp 3'