Canonical Allele Identifier: CA869715821
Gene: MORC4 HGNC NCBI

Linked Data

dbSNP Id: rs1345235875
gnomAD v3: X-106940510-A-G
gnomAD v4: X-106940510-A-G
MyVariant Identifiers: chrX:g.106183740A>G (hg19) chrX:g.106940510A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106940510A>G , CM000685.2:g.106940510A>G GRCh38
NC_000023.10:g.106183740A>G , CM000685.1:g.106183740A>G GRCh37
NC_000023.9:g.106070396A>G NCBI36
NG_016392.1:g.64735T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000604604.1:c.111+52720T>C
XM_005262190.3:c.*969T>C XP_005262247.1:n.*969T>C
XM_006724691.2:c.*969T>C XP_006724754.1:n.*969T>C
XM_011531027.2:c.*969T>C XP_011529329.1:n.*969T>C
XM_017029844.1:c.*1042T>C XP_016885333.1:n.*1042T>C
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