Canonical Allele Identifier: CA1157148704
Gene: MICOS10 HGNC NCBI

Linked Data

dbSNP Id: rs1570418090

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19517064A>C , CM000663.2:g.19517064A>C GRCh38
NC_000001.10:g.19843558A>C , CM000663.1:g.19843558A>C GRCh37
NC_000001.9:g.19716145A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648702.1:c.-54+32409A>C ENSP00000497006.1:n.-54+32409A>C
XR_947017.1:n.372+1019T>G
XR_947019.1:n.189-1057A>C
XR_947020.1:n.144-1057A>C
XR_001737920.1:n.144-1057A>C
XR_947017.2:n.1178+1019T>G
XR_947020.2:n.144-1057A>C