Canonical Allele Identifier: CA1138567026
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066910674
gnomAD v3: X-154097877-A-AG
gnomAD v4: X-154097877-A-AG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097883dup , CM000685.2:g.154097883dup GRCh38
NC_000023.10:g.153363340dup , CM000685.1:g.153363340dup GRCh37
NC_000023.9:g.153016534dup NCBI36
NG_007107.2:g.44244dup
NG_007107.3:g.44226dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6903dup
Search 100 bp 5'
Search 100 bp 3'