Canonical Allele Identifier: CA2466594938
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066910467

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097872G>A , CM000685.2:g.154097872G>A GRCh38
NC_000023.10:g.153363329G>A , CM000685.1:g.153363329G>A GRCh37
NC_000023.9:g.153016523G>A NCBI36
NG_007107.2:g.44250C>T
NG_007107.3:g.44232C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6909C>T