Canonical Allele Identifier: CA2466594955
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066910781

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097882G>T , CM000685.2:g.154097882G>T GRCh38
NC_000023.10:g.153363339G>T , CM000685.1:g.153363339G>T GRCh37
NC_000023.9:g.153016533G>T NCBI36
NG_007107.2:g.44240C>A
NG_007107.3:g.44222C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6899C>A