Canonical Allele Identifier: CA729501423
Gene: MICOS10 HGNC NCBI

Linked Data

dbSNP Id: rs1232849069
MyVariant Identifiers: chr1:g.19843521G>A (hg19) chr1:g.19517027G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19517027G>A , CM000663.2:g.19517027G>A GRCh38
NC_000001.10:g.19843521G>A , CM000663.1:g.19843521G>A GRCh37
NC_000001.9:g.19716108G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000648702.1:c.-54+32372G>A ENSP00000497006.1:n.-54+32372G>A
XR_947017.1:n.372+1056C>T
XR_947019.1:n.189-1094G>A
XR_947020.1:n.144-1094G>A
XR_001737920.1:n.144-1094G>A
XR_947017.2:n.1178+1056C>T
XR_947020.2:n.144-1094G>A
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