Canonical Allele Identifier: CA1946721132
Gene: ECHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1849145548

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373365A>G , CM000672.2:g.133373365A>G GRCh38
NC_000010.10:g.135186869A>G , CM000672.1:g.135186869A>G GRCh37
NC_000010.9:g.135036859A>G NCBI36
NG_042077.1:g.5040T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.3:c.-32T>C ENSP00000357535.3:n.-32T>C
NM_004092.3:c.-32T>C NP_004083.3:n.-32T>C
XR_002956965.1:n.32T>C