Canonical Allele Identifier: CA2602677642
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2148771408
gnomAD v3: X-154097934-C-T
gnomAD v4: X-154097934-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097934C>T , CM000685.2:g.154097934C>T GRCh38
NC_000023.10:g.153363392C>T , CM000685.1:g.153363392C>T GRCh37
NC_000023.9:g.153016586C>T NCBI36
NG_007107.2:g.44187G>A
NG_007107.3:g.44170G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6847G>A
Search 100 bp 5'
Search 100 bp 3'