Canonical Allele Identifier: CA2611598722
Gene: ECHS1 HGNC NCBI

Linked Data

gnomAD v4: 10-133373401-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373401C>A , CM000672.2:g.133373401C>A GRCh38
NC_000010.10:g.135186905C>A , CM000672.1:g.135186905C>A GRCh37
NC_000010.9:g.135036895C>A NCBI36
NG_042077.1:g.5004G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.3:c.-68G>T ENSP00000357535.3:n.-68G>T
NM_004092.3:c.-68G>T NP_004083.3:n.-68G>T
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