Canonical Allele Identifier: CA2466594933
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066910383

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097869del , CM000685.2:g.154097869del GRCh38
NC_000023.10:g.153363326del , CM000685.1:g.153363326del GRCh37
NC_000023.9:g.153016520del NCBI36
NG_007107.2:g.44254del
NG_007107.3:g.44236del

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6913del