Canonical Allele Identifier: CA2695105728
Gene: MECP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097870A>G , CM000685.2:g.154097870A>G GRCh38
NC_000023.10:g.153363327A>G , CM000685.1:g.153363327A>G GRCh37
NC_000023.9:g.153016521A>G NCBI36
NG_007107.2:g.44252T>C
NG_007107.3:g.44234T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6911T>C