Canonical Allele Identifier: CA2695105768
Gene: MECP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097908T>C , CM000685.2:g.154097908T>C GRCh38
NC_000023.10:g.153363366T>C , CM000685.1:g.153363366T>C GRCh37
NC_000023.9:g.153016560T>C NCBI36
NG_007107.2:g.44213A>G
NG_007107.3:g.44196A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6873A>G