Canonical Allele Identifier: CA1946721179
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373427C= , CM000672.2:g.133373427C= GRCh38
NC_000010.10:g.135186931C= , CM000672.1:g.135186931C= GRCh37
NC_000010.9:g.135036921C= NCBI36
NG_042077.1:g.4978G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.3:c.-94G= ENSP00000357535.3:n.-94G=