Canonical Allele Identifier: CA2611598766
Gene: ECHS1 HGNC NCBI

Linked Data

gnomAD v4: 10-133373427-C-G
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Genomic Alleles

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

Transcript Alleles

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