Canonical Allele Identifier: CA2695105611
Gene: MECP2 HGNC NCBI

Linked Data

gnomAD v4: X-154097763-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097763T>A , CM000685.2:g.154097763T>A GRCh38
NC_000023.10:g.153363220T>A , CM000685.1:g.153363220T>A GRCh37
NC_000023.9:g.153016414T>A NCBI36
NG_007107.2:g.44359A>T
NG_007107.3:g.44341A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453960.6:c.-98A>T ENSP00000395535.2:n.-98A>T
ENST00000631210.1:n.305+7018A>T
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