Canonical Allele Identifier: CA2611598785
Gene: ECHS1 HGNC NCBI

Linked Data

gnomAD v4: 10-133373435-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373435C>T , CM000672.2:g.133373435C>T GRCh38
NC_000010.10:g.135186939C>T , CM000672.1:g.135186939C>T GRCh37
NC_000010.9:g.135036929C>T NCBI36
NG_042077.1:g.4970G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.3:c.-102G>A ENSP00000357535.3:n.-102G>A
Search 100 bp 5'
Search 100 bp 3'