Canonical Allele Identifier: CA729501392
Gene: MICOS10 HGNC NCBI

Linked Data

dbSNP Id: rs1309981929
gnomAD v3: 1-19516989-C-G
gnomAD v4: 1-19516989-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19516989C>G , CM000663.2:g.19516989C>G GRCh38
NC_000001.10:g.19843483C>G , CM000663.1:g.19843483C>G GRCh37
NC_000001.9:g.19716070C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648702.1:c.-54+32334C>G ENSP00000497006.1:n.-54+32334C>G
XR_947017.1:n.372+1094G>C
XR_947019.1:n.189-1132C>G
XR_947020.1:n.144-1132C>G
XR_001737920.1:n.144-1132C>G
XR_947017.2:n.1178+1094G>C
XR_947020.2:n.144-1132C>G