Canonical Allele Identifier: CA869715873
Gene: MORC4 HGNC NCBI

Linked Data

dbSNP Id: rs1481296834
MyVariant Identifiers: chrX:g.106183847C>A (hg19) chrX:g.106940617C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106940617C>A , CM000685.2:g.106940617C>A GRCh38
NC_000023.10:g.106183847C>A , CM000685.1:g.106183847C>A GRCh37
NC_000023.9:g.106070503C>A NCBI36
NG_016392.1:g.64628G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000604604.1:c.111+52613G>T
XM_005262190.3:c.*862G>T XP_005262247.1:n.*862G>T
XM_006724691.2:c.*862G>T XP_006724754.1:n.*862G>T
XM_011531027.2:c.*862G>T XP_011529329.1:n.*862G>T
XM_017029844.1:c.*935G>T XP_016885333.1:n.*935G>T
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