Canonical Allele Identifier: CA337660524
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs192241610
MyVariant Identifiers: chrX:g.153363302T>G (hg19) chrX:g.154097845T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097845T>G , CM000685.2:g.154097845T>G GRCh38
NC_000023.10:g.153363302T>G , CM000685.1:g.153363302T>G GRCh37
NC_000023.9:g.153016496T>G NCBI36
NG_007107.2:g.44277A>C
NG_007107.3:g.44259A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6936A>C
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