Canonical Allele Identifier: CA873306116
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1324690647
gnomAD v3: X-154097883-G-T
gnomAD v4: X-154097883-G-T
MyVariant Identifiers: chrX:g.154097883G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097883G>T , CM000685.2:g.154097883G>T GRCh38
NC_000023.10:g.153363340G>T , CM000685.1:g.153363340G>T GRCh37
NC_000023.9:g.153016534G>T NCBI36
NG_007107.2:g.44239C>A
NG_007107.3:g.44221C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6898C>A
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