Canonical Allele Identifier: CA5765923
Gene: ECHS1 HGNC NCBI

Linked Data

dbSNP Id: rs765896234
ExAC: 10:135186835 C / T
gnomAD v2: 10-135186835-C-T
gnomAD v4: 10-133373331-C-T
MyVariant Identifiers: chr10:g.135186835C>T (hg19) chr10:g.133373331C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373331C>T , CM000672.2:g.133373331C>T GRCh38
NC_000010.10:g.135186835C>T , CM000672.1:g.135186835C>T GRCh37
NC_000010.9:g.135036825C>T NCBI36
NG_042077.1:g.5074G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.3G>A MANE Select ENSP00000357535.3:p.Met1Ile
ENST00000368547.3:c.3G>A ENSP00000357535.3:p.Met1Ile
NM_004092.3:c.3G>A NP_004083.3:p.Met1Ile
XR_002956965.1:n.66G>A
NM_004092.4:c.3G>A MANE Select NP_004083.3:p.Met1Ile
Search 100 bp 5'
Search 100 bp 3'