Canonical Allele Identifier: CA333029250
Gene: MORC4 HGNC NCBI

Linked Data

dbSNP Id: rs899075908
gnomAD v3: X-106940478-C-T
gnomAD v4: X-106940478-C-T
MyVariant Identifiers: chrX:g.106183708C>T (hg19) chrX:g.106940478C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106940478C>T , CM000685.2:g.106940478C>T GRCh38
NC_000023.10:g.106183708C>T , CM000685.1:g.106183708C>T GRCh37
NC_000023.9:g.106070364C>T NCBI36
NG_016392.1:g.64767G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000604604.1:c.111+52752G>A
XM_005262190.3:c.*1001G>A XP_005262247.1:n.*1001G>A
XM_006724691.2:c.*1001G>A XP_006724754.1:n.*1001G>A
XM_011531027.2:c.*1001G>A XP_011529329.1:n.*1001G>A
XM_017029844.1:c.*1074G>A XP_016885333.1:n.*1074G>A
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