Canonical Allele Identifier: CA2466594876
Gene: MECP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097785T= , CM000685.2:g.154097785T= GRCh38
NC_000023.10:g.153363242T= , CM000685.1:g.153363242T= GRCh37
NC_000023.9:g.153016436T= NCBI36
NG_007107.2:g.44337A=
NG_007107.3:g.44319A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6996A=