Canonical Allele Identifier: CA2466594900
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs2066909639
gnomAD v4: X-154097828-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097828C>T , CM000685.2:g.154097828C>T GRCh38
NC_000023.10:g.153363285C>T , CM000685.1:g.153363285C>T GRCh37
NC_000023.9:g.153016479C>T NCBI36
NG_007107.2:g.44294G>A
NG_007107.3:g.44276G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6953G>A
Search 100 bp 5'
Search 100 bp 3'