Canonical Allele Identifier: CA645228311
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1335947315
gnomAD v2: X-153363330-G-A
gnomAD v3: X-154097873-G-A
gnomAD v4: X-154097873-G-A
MyVariant Identifiers: chrX:g.153363330G>A (hg19) chrX:g.154097873G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097873G>A , CM000685.2:g.154097873G>A GRCh38
NC_000023.10:g.153363330G>A , CM000685.1:g.153363330G>A GRCh37
NC_000023.9:g.153016524G>A NCBI36
NG_007107.2:g.44249C>T
NG_007107.3:g.44231C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6908C>T
Search 100 bp 5'
Search 100 bp 3'