Canonical Allele Identifier: CA337660526

Gene: MECP2

Linked Data

• dbSNP Id: rs373337264
• MyVariant Identifiers: chrX:g.154097884A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097884A>G , CM000685.2:g.154097884A>G	GRCh38
NG_007107.3:g.44220T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631210.1:n.305+6897T>C