Canonical Allele Identifier: CA873306040
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1224856339
gnomAD v3: X-154097766-T-A
gnomAD v4: X-154097766-T-A
MyVariant Identifiers: chrX:g.154097766T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097766T>A , CM000685.2:g.154097766T>A GRCh38
NC_000023.10:g.153363223T>A , CM000685.1:g.153363223T>A GRCh37
NC_000023.9:g.153016417T>A NCBI36
NG_007107.2:g.44356A>T
NG_007107.3:g.44338A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+7015A>T
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