Canonical Allele Identifier: CA337660534

Gene: MECP2

Linked Data

• dbSNP Id: rs893158200
• MyVariant Identifiers: chrX:g.154097939A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097939A>G , CM000685.2:g.154097939A>G	GRCh38
NC_000023.10:g.153363397A>G , CM000685.1:g.153363397A>G	GRCh37
NC_000023.9:g.153016591A>G	NCBI36
NG_007107.2:g.44182T>C
NG_007107.3:g.44165T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631210.1:n.305+6842T>C