Canonical Allele Identifier: CA2695105767
Gene: MECP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097907T>C , CM000685.2:g.154097907T>C GRCh38
NC_000023.10:g.153363365T>C , CM000685.1:g.153363365T>C GRCh37
NC_000023.9:g.153016559T>C NCBI36
NG_007107.2:g.44214A>G
NG_007107.3:g.44197A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6874A>G