Canonical Allele Identifier: CA2524963805

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6909805C>T , CM000686.2:g.6909805C>T GRCh38
NC_000024.9:g.6777846C>T , CM000686.1:g.6777846C>T GRCh37
NC_000024.8:g.6837846C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.-113+1868G>A (AMELY) MANE Select ENSP00000498344.1:n.-113+1868G>A
ENST00000651267.1:c.-113+1868G>A (AMELY) ENSP00000498344.1:n.-113+1868G>A
XM_011531472.1:c.-113+1868G>A (AMELY) XP_011529774.1:n.-113+1868G>A
XM_024452497.1:c.-649C>T (TBL1Y) XP_024308265.1:n.-649C>T
NM_001143.2:c.-113+1868G>A (AMELY) MANE Select NP_001134.1:n.-113+1868G>A