Canonical Allele Identifier: CA19197852
Gene: MICOS10 HGNC NCBI

Linked Data

dbSNP Id: rs10917469
gnomAD v2: 1-19843576-A-G
gnomAD v3: 1-19517082-A-G
gnomAD v4: 1-19517082-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19517082A>G , CM000663.2:g.19517082A>G GRCh38
NC_000001.10:g.19843576A>G , CM000663.1:g.19843576A>G GRCh37
NC_000001.9:g.19716163A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000648702.1:c.-54+32427A>G ENSP00000497006.1:n.-54+32427A>G
XR_947017.1:n.372+1001T>C
XR_947019.1:n.189-1039A>G
XR_947020.1:n.144-1039A>G
XR_001737920.1:n.144-1039A>G
XR_947017.2:n.1178+1001T>C
XR_947020.2:n.144-1039A>G