Canonical Allele Identifier: CA19197830
Gene: MICOS10 HGNC NCBI

Linked Data

dbSNP Id: rs183025727
gnomAD v2: 1-19843526-G-A
gnomAD v3: 1-19517032-G-A
gnomAD v4: 1-19517032-G-A
MyVariant Identifiers: chr1:g.19843526G>A (hg19) chr1:g.19517032G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19517032G>A , CM000663.2:g.19517032G>A GRCh38
NC_000001.10:g.19843526G>A , CM000663.1:g.19843526G>A GRCh37
NC_000001.9:g.19716113G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648702.1:c.-54+32377G>A ENSP00000497006.1:n.-54+32377G>A
XR_947017.1:n.372+1051C>T
XR_947019.1:n.189-1089G>A
XR_947020.1:n.144-1089G>A
XR_001737920.1:n.144-1089G>A
XR_947017.2:n.1178+1051C>T
XR_947020.2:n.144-1089G>A
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