Canonical Allele Identifier: CA1138567061

Gene: MECP2

Linked Data

• dbSNP Id: rs2066911180
• gnomAD v3: X-154097902-G-C
• gnomAD v4: X-154097902-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154097902G>C , CM000685.2:g.154097902G>C	GRCh38
NC_000023.10:g.153363360G>C , CM000685.1:g.153363360G>C	GRCh37
NC_000023.9:g.153016554G>C	NCBI36
NG_007107.2:g.44219C>G
NG_007107.3:g.44202C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631210.1:n.305+6879C>G