Canonical Allele Identifier: CA1946721178
Gene: ECHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1589885034

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373426C>T , CM000672.2:g.133373426C>T GRCh38
NC_000010.10:g.135186930C>T , CM000672.1:g.135186930C>T GRCh37
NC_000010.9:g.135036920C>T NCBI36
NG_042077.1:g.4979G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.3:c.-93G>A ENSP00000357535.3:n.-93G>A