Canonical Allele Identifier: CA1946721191
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373445T= , CM000672.2:g.133373445T= GRCh38
NC_000010.10:g.135186949T= , CM000672.1:g.135186949T= GRCh37
NC_000010.9:g.135036939T= NCBI36
NG_042077.1:g.4960A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.3:c.-112A= ENSP00000357535.3:n.-112A=