Canonical Allele Identifier: CA2695105775
Gene: MECP2 HGNC NCBI

Linked Data

gnomAD v4: X-154097913-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097913A>G , CM000685.2:g.154097913A>G GRCh38
NC_000023.10:g.153363371A>G , CM000685.1:g.153363371A>G GRCh37
NC_000023.9:g.153016565A>G NCBI36
NG_007107.2:g.44208T>C
NG_007107.3:g.44191T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6868T>C
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