Canonical Allele Identifier: CA472230268
Gene: ECHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1279794402
gnomAD v2: 10-135186817-C-G
gnomAD v3: 10-133373313-C-G
gnomAD v4: 10-133373313-C-G
MyVariant Identifiers: chr10:g.135186817C>G (hg19) chr10:g.133373313C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373313C>G , CM000672.2:g.133373313C>G GRCh38
NC_000010.10:g.135186817C>G , CM000672.1:g.135186817C>G GRCh37
NC_000010.9:g.135036807C>G NCBI36
NG_042077.1:g.5092G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.21G>C MANE Select ENSP00000357535.3:p.Leu7=
ENST00000368547.3:c.21G>C ENSP00000357535.3:p.Leu7=
NM_004092.3:c.21G>C NP_004083.3:p.Leu7=
XR_002956965.1:n.84G>C
NM_004092.4:c.21G>C MANE Select NP_004083.3:p.Leu7=
Search 100 bp 5'
Search 100 bp 3'