Canonical Allele Identifier: CA869715711
Gene: MORC4 HGNC NCBI

Linked Data

dbSNP Id: rs1206275943
gnomAD v3: X-106940333-G-C
gnomAD v4: X-106940333-G-C
MyVariant Identifiers: chrX:g.106183563G>C (hg19) chrX:g.106940333G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106940333G>C , CM000685.2:g.106940333G>C GRCh38
NC_000023.10:g.106183563G>C , CM000685.1:g.106183563G>C GRCh37
NC_000023.9:g.106070219G>C NCBI36
NG_016392.1:g.64912C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000604604.1:c.111+52897C>G
XM_005262190.3:c.*1146C>G XP_005262247.1:n.*1146C>G
XM_006724691.2:c.*1146C>G XP_006724754.1:n.*1146C>G
XM_011531027.2:c.*1146C>G XP_011529329.1:n.*1146C>G
XM_017029844.1:c.*1219C>G XP_016885333.1:n.*1219C>G
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