Canonical Allele Identifier: CA1138838518
Gene: AMELY HGNC NCBI
TBL1Y HGNC NCBI

Linked Data

gnomAD v3: Y-6909802-G-C
gnomAD v4: Y-6909802-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6909802G>C , CM000686.2:g.6909802G>C GRCh38
NC_000024.9:g.6777843G>C , CM000686.1:g.6777843G>C GRCh37
NC_000024.8:g.6837843G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.-113+1871C>G (AMELY) MANE Select ENSP00000498344.1:n.-113+1871C>G
ENST00000651267.1:c.-113+1871C>G (AMELY) ENSP00000498344.1:n.-113+1871C>G
XM_011531472.1:c.-113+1871C>G (AMELY) XP_011529774.1:n.-113+1871C>G
XM_024452497.1:c.-652G>C (TBL1Y) XP_024308265.1:n.-652G>C
NM_001143.2:c.-113+1871C>G (AMELY) MANE Select NP_001134.1:n.-113+1871C>G
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