Canonical Allele Identifier: CA2466594988
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1603341458

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097946G>T , CM000685.2:g.154097946G>T GRCh38
NC_000023.10:g.153363404G>T , CM000685.1:g.153363404G>T GRCh37
NC_000023.9:g.153016598G>T NCBI36
NG_007107.2:g.44175C>A
NG_007107.3:g.44158C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6835C>A