Canonical Allele Identifier: CA2611598714
Gene: ECHS1 HGNC NCBI

Linked Data

gnomAD v4: 10-133373395-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373395C>G , CM000672.2:g.133373395C>G GRCh38
NC_000010.10:g.135186899C>G , CM000672.1:g.135186899C>G GRCh37
NC_000010.9:g.135036889C>G NCBI36
NG_042077.1:g.5010G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.3:c.-62G>C ENSP00000357535.3:n.-62G>C
NM_004092.3:c.-62G>C NP_004083.3:n.-62G>C
XR_002956965.1:n.2G>C
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