Canonical Allele Identifier: CA337660535
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs893158200
gnomAD v3: X-154097939-A-T
gnomAD v4: X-154097939-A-T
MyVariant Identifiers: chrX:g.154097939A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097939A>T , CM000685.2:g.154097939A>T GRCh38
NC_000023.10:g.153363397A>T , CM000685.1:g.153363397A>T GRCh37
NC_000023.9:g.153016591A>T NCBI36
NG_007107.2:g.44182T>A
NG_007107.3:g.44165T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6842T>A
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