Canonical Allele Identifier: CA1138567003
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1475414282
gnomAD v3: X-154097847-A-G
gnomAD v4: X-154097847-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097847A>G , CM000685.2:g.154097847A>G GRCh38
NC_000023.10:g.153363304A>G , CM000685.1:g.153363304A>G GRCh37
NC_000023.9:g.153016498A>G NCBI36
NG_007107.2:g.44275T>C
NG_007107.3:g.44257T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6934T>C
Search 100 bp 5'
Search 100 bp 3'