Canonical Allele Identifier: CA1157148731
Gene: MICOS10 HGNC NCBI

Linked Data

dbSNP Id: rs2094698623

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19517144G>A , CM000663.2:g.19517144G>A GRCh38
NC_000001.10:g.19843638G>A , CM000663.1:g.19843638G>A GRCh37
NC_000001.9:g.19716225G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648702.1:c.-54+32489G>A ENSP00000497006.1:n.-54+32489G>A
XR_947017.1:n.372+939C>T
XR_947019.1:n.189-977G>A
XR_947020.1:n.144-977G>A
XR_001737920.1:n.144-977G>A
XR_947017.2:n.1178+939C>T
XR_947020.2:n.144-977G>A