Canonical Allele Identifier: CA2466594995
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066911825

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097960G>A , CM000685.2:g.154097960G>A GRCh38
NC_000023.10:g.153363418G>A , CM000685.1:g.153363418G>A GRCh37
NC_000023.9:g.153016612G>A NCBI36
NG_007107.2:g.44161C>T
NG_007107.3:g.44144C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6821C>T