Canonical Allele Identifier: CA314656468

Gene: CTNNBL1

Linked Data

• dbSNP Id: rs968142598
• gnomAD v3: 20-37712665-A-G
• gnomAD v4: 20-37712665-A-G
• MyVariant Identifiers: chr20:g.36341067A>G (hg19) ; chr20:g.37712665A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37712665A>G , CM000682.2:g.37712665A>G	GRCh38
NC_000020.10:g.36341067A>G , CM000682.1:g.36341067A>G	GRCh37
NC_000020.9:g.35774481A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361383.11:c.30+18513A>G MANE Select	ENSP00000355050.6:n.30+18513A>G
ENST00000361383.10:c.30+18513A>G	ENSP00000355050.6:n.30+18513A>G
ENST00000405275.6:c.-152-14637A>G	ENSP00000384355.2:n.-152-14637A>G
ENST00000447935.3:c.-52+17632A>G	ENSP00000394464.1:n.-52+17632A>G
ENST00000621317.4:c.30+18513A>G	ENSP00000478532.1:n.30+18513A>G
ENST00000628103.2:c.-152-14637A>G	ENSP00000487198.1:n.-152-14637A>G
NM_001281495.1:c.-152-14637A>G	NP_001268424.1:n.-152-14637A>G
NM_030877.4:c.30+18513A>G	NP_110517.2:n.30+18513A>G
XM_024451947.1:c.-52+17632A>G	XP_024307715.1:n.-52+17632A>G
NM_030877.5:c.30+18513A>G MANE Select	NP_110517.2:n.30+18513A>G
NM_001281495.2:c.-152-14637A>G	NP_001268424.1:n.-152-14637A>G