Canonical Allele Identifier: CA645228307
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs192241610
gnomAD v2: X-153363302-T-C
gnomAD v3: X-154097845-T-C
gnomAD v4: X-154097845-T-C
MyVariant Identifiers: chrX:g.153363302T>C (hg19) chrX:g.154097845T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6936A>G
Search 100 bp 5'
Search 100 bp 3'