Canonical Allele Identifier: CA2466594909
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066909830

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097843T>C , CM000685.2:g.154097843T>C GRCh38
NC_000023.10:g.153363300T>C , CM000685.1:g.153363300T>C GRCh37
NC_000023.9:g.153016494T>C NCBI36
NG_007107.2:g.44279A>G
NG_007107.3:g.44261A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6938A>G