Canonical Allele Identifier: CA1946721114
Gene: ECHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1849144997
gnomAD v4: 10-133373348-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373348C>T , CM000672.2:g.133373348C>T GRCh38
NC_000010.10:g.135186852C>T , CM000672.1:g.135186852C>T GRCh37
NC_000010.9:g.135036842C>T NCBI36
NG_042077.1:g.5057G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.-15G>A MANE Select ENSP00000357535.3:n.-15G>A
ENST00000368547.3:c.-15G>A ENSP00000357535.3:n.-15G>A
NM_004092.3:c.-15G>A NP_004083.3:n.-15G>A
XR_002956965.1:n.49G>A
NM_004092.4:c.-15G>A MANE Select NP_004083.3:n.-15G>A
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