Canonical Allele Identifier: CA472230372
Gene: ECHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1204597554
gnomAD v2: 10-135186842-C-T
gnomAD v3: 10-133373338-C-T
gnomAD v4: 10-133373338-C-T
MyVariant Identifiers: chr10:g.135186842C>T (hg19) chr10:g.133373338C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373338C>T , CM000672.2:g.133373338C>T GRCh38
NC_000010.10:g.135186842C>T , CM000672.1:g.135186842C>T GRCh37
NC_000010.9:g.135036832C>T NCBI36
NG_042077.1:g.5067G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.-5G>A MANE Select ENSP00000357535.3:n.-5G>A
ENST00000368547.3:c.-5G>A ENSP00000357535.3:n.-5G>A
NM_004092.3:c.-5G>A NP_004083.3:n.-5G>A
XR_002956965.1:n.59G>A
NM_004092.4:c.-5G>A MANE Select NP_004083.3:n.-5G>A
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