Canonical Allele Identifier: CA873306033
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1256446715
MyVariant Identifiers: chrX:g.154097740A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097740A>G , CM000685.2:g.154097740A>G GRCh38
NC_000023.10:g.153363197A>G , CM000685.1:g.153363197A>G GRCh37
NC_000023.9:g.153016391A>G NCBI36
NG_007107.2:g.44382T>C
NG_007107.3:g.44364T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303391.10:c.-235T>C ENSP00000301948.6:n.-235T>C
ENST00000453960.6:c.-75T>C ENSP00000395535.2:n.-75T>C
ENST00000631210.1:n.305+7041T>C