Canonical Allele Identifier: CA2466594915
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066909997

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097855_154097856insGGAGGGGGGAGTCT , CM000685.2:g.154097855_154097856insGGAGGGGGGAGTCT GRCh38
NC_000023.10:g.153363312_153363313insGGAGGGGGGAGTCT , CM000685.1:g.153363312_153363313insGGAGGGGGGAGTCT GRCh37
NC_000023.9:g.153016506_153016507insGGAGGGGGGAGTCT NCBI36
NG_007107.2:g.44266_44267insAGACTCCCCCCTCC
NG_007107.3:g.44248_44249insAGACTCCCCCCTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6925_305+6926insAGACTCCCCCCTCC