Canonical Allele Identifier: CA1017382342
Gene: CTNNBL1 HGNC NCBI

Linked Data

gnomAD v3: 20-37712688-T-A
gnomAD v4: 20-37712688-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.37712688T>A , CM000682.2:g.37712688T>A GRCh38
NC_000020.10:g.36341090T>A , CM000682.1:g.36341090T>A GRCh37
NC_000020.9:g.35774504T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361383.11:c.30+18536T>A MANE Select ENSP00000355050.6:n.30+18536T>A
ENST00000361383.10:c.30+18536T>A ENSP00000355050.6:n.30+18536T>A
ENST00000405275.6:c.-152-14614T>A ENSP00000384355.2:n.-152-14614T>A
ENST00000447935.3:c.-52+17655T>A ENSP00000394464.1:n.-52+17655T>A
ENST00000621317.4:c.30+18536T>A ENSP00000478532.1:n.30+18536T>A
ENST00000628103.2:c.-152-14614T>A ENSP00000487198.1:n.-152-14614T>A
NM_001281495.1:c.-152-14614T>A NP_001268424.1:n.-152-14614T>A
NM_030877.4:c.30+18536T>A NP_110517.2:n.30+18536T>A
XM_024451947.1:c.-52+17655T>A XP_024307715.1:n.-52+17655T>A
NM_030877.5:c.30+18536T>A MANE Select NP_110517.2:n.30+18536T>A
NM_001281495.2:c.-152-14614T>A NP_001268424.1:n.-152-14614T>A
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