Canonical Allele Identifier: CA645228310
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1444776004
gnomAD v2: X-153363322-G-A
gnomAD v4: X-154097865-G-A
MyVariant Identifiers: chrX:g.153363322G>A (hg19) chrX:g.154097865G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097865G>A , CM000685.2:g.154097865G>A GRCh38
NC_000023.10:g.153363322G>A , CM000685.1:g.153363322G>A GRCh37
NC_000023.9:g.153016516G>A NCBI36
NG_007107.2:g.44257C>T
NG_007107.3:g.44239C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6916C>T
Search 100 bp 5'
Search 100 bp 3'