Canonical Allele Identifier: CA333029333
Gene: MORC4 HGNC NCBI

Linked Data

dbSNP Id: rs957814765
gnomAD v3: X-106940659-T-A
gnomAD v4: X-106940659-T-A
MyVariant Identifiers: chrX:g.106183889T>A (hg19) chrX:g.106940659T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106940659T>A , CM000685.2:g.106940659T>A GRCh38
NC_000023.10:g.106183889T>A , CM000685.1:g.106183889T>A GRCh37
NC_000023.9:g.106070545T>A NCBI36
NG_016392.1:g.64586A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000604604.1:c.111+52571A>T
XM_005262190.3:c.*820A>T XP_005262247.1:n.*820A>T
XM_006724691.2:c.*820A>T XP_006724754.1:n.*820A>T
XM_011531027.2:c.*820A>T XP_011529329.1:n.*820A>T
XM_017029844.1:c.*893A>T XP_016885333.1:n.*893A>T
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