Canonical Allele Identifier: CA15094653
Gene: LGR6 HGNC NCBI

Linked Data

dbSNP Id: rs6678914
gnomAD v2: 1-202187176-G-A
gnomAD v3: 1-202218048-G-A
gnomAD v4: 1-202218048-G-A
MyVariant Identifiers: chr1:g.202187176G>A (hg19) chr1:g.202218048G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202218048G>A , CM000663.2:g.202218048G>A GRCh38
NC_000001.10:g.202187176G>A , CM000663.1:g.202187176G>A GRCh37
NC_000001.9:g.200453799G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000367278.8:c.213-7375G>A MANE Select ENSP00000356247.3:n.213-7375G>A
ENST00000255432.11:c.57-7375G>A ENSP00000255432.7:n.57-7375G>A
ENST00000367278.7:c.213-7375G>A ENSP00000356247.3:n.213-7375G>A
ENST00000423542.5:c.-11+7257G>A ENSP00000402284.1:n.-11+7257G>A
ENST00000439764.2:c.83+3811G>A ENSP00000387869.2:n.83+3811G>A
ENST00000487787.5:c.57-7375G>A ENSP00000422143.1:n.57-7375G>A
NM_001017403.1:c.213-7375G>A NP_001017403.1:n.213-7375G>A
NM_001017404.1:c.83+3811G>A NP_001017404.1:n.83+3811G>A
NM_021636.2:c.57-7375G>A NP_067649.2:n.57-7375G>A
XM_005245404.2:c.83+3811G>A XP_005245461.1:n.83+3811G>A
XM_011509838.1:c.83+3811G>A XP_011508140.1:n.83+3811G>A
XM_011509839.1:c.83+3811G>A XP_011508141.1:n.83+3811G>A
XM_011509840.1:c.83+3811G>A XP_011508142.1:n.83+3811G>A
XM_005245404.3:c.83+3811G>A XP_005245461.1:n.83+3811G>A
XM_011509838.2:c.83+3811G>A XP_011508140.1:n.83+3811G>A
XM_011509839.2:c.83+3811G>A XP_011508141.1:n.83+3811G>A
XM_011509840.2:c.83+3811G>A XP_011508142.1:n.83+3811G>A
XM_017001996.1:c.83+3811G>A XP_016857485.1:n.83+3811G>A
NM_021636.3:c.57-7375G>A NP_067649.2:n.57-7375G>A
NM_001017403.2:c.213-7375G>A MANE Select NP_001017403.1:n.213-7375G>A
NM_001017404.2:c.83+3811G>A NP_001017404.1:n.83+3811G>A
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