Canonical Allele Identifier: CA645228315
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1557151013
gnomAD v2: X-153363392-CAGGGA-C
MyVariant Identifiers: chrX:g.153363393_153363397del (hg19) chrX:g.154097935_154097939del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097936_154097940del , CM000685.2:g.154097936_154097940del GRCh38
NC_000023.10:g.153363394_153363398del , CM000685.1:g.153363394_153363398del GRCh37
NC_000023.9:g.153016588_153016592del NCBI36
NG_007107.2:g.44182_44186del
NG_007107.3:g.44165_44169del

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6842_305+6846del
Search 100 bp 5'
Search 100 bp 3'