Canonical Allele Identifier: CA2602677640

Gene: MECP2

Linked Data

• dbSNP Id: rs1054443386
• gnomAD v3: X-154097926-A-G
• gnomAD v4: X-154097926-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097926A>G , CM000685.2:g.154097926A>G	GRCh38
NC_000023.10:g.153363384A>G , CM000685.1:g.153363384A>G	GRCh37
NC_000023.9:g.153016578A>G	NCBI36
NG_007107.2:g.44195T>C
NG_007107.3:g.44178T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631210.1:n.305+6855T>C