Canonical Allele Identifier: CA645228314

Gene: MECP2

Linked Data

• dbSNP Id: rs1557151005
• gnomAD v2: X-153363343-GT-G
• MyVariant Identifiers: chrX:g.153363344del (hg19) ; chrX:g.154097886del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097886del , CM000685.2:g.154097886del	GRCh38
NC_000023.10:g.153363344del , CM000685.1:g.153363344del	GRCh37
NC_000023.9:g.153016538del	NCBI36
NG_007107.2:g.44235del
NG_007107.3:g.44218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631210.1:n.305+6895del