Canonical Allele Identifier: CA645228317
Gene: MECP2 HGNC NCBI

Linked Data

dbSNP Id: rs1557151027
gnomAD v2: X-153363437-C-T
gnomAD v3: X-154097979-C-T
gnomAD v4: X-154097979-C-T
MyVariant Identifiers: chrX:g.153363437C>T (hg19) chrX:g.154097979C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154097979C>T , CM000685.2:g.154097979C>T GRCh38
NC_000023.10:g.153363437C>T , CM000685.1:g.153363437C>T GRCh37
NC_000023.9:g.153016631C>T NCBI36
NG_007107.2:g.44142G>A
NG_007107.3:g.44125G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000631210.1:n.305+6802G>A
Search 100 bp 5'
Search 100 bp 3'