Canonical Allele Identifier: CA556938564
Gene: TENM3 HGNC NCBI

Linked Data

dbSNP Id: rs1389641730
gnomAD v2: 4-182609806-C-A
gnomAD v3: 4-181688653-C-A
gnomAD v4: 4-181688653-C-A
MyVariant Identifiers: chr4:g.182609806C>A (hg19) chr4:g.181688653C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.181688653C>A , CM000666.2:g.181688653C>A GRCh38
NC_000004.11:g.182609806C>A , CM000666.1:g.182609806C>A GRCh37
NC_000004.10:g.182846800C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939532.1:n.155-50834C>A
XM_017008385.1:c.-399-50834C>A XP_016863874.1:n.-399-50834C>A
XM_017008389.1:c.-399-50834C>A XP_016863878.1:n.-399-50834C>A
XM_017008390.1:c.-399-50834C>A XP_016863879.1:n.-399-50834C>A
XM_017008391.1:c.-399-50834C>A XP_016863880.1:n.-399-50834C>A
XM_017008392.1:c.-399-50834C>A XP_016863881.1:n.-399-50834C>A
XM_017008393.1:c.-399-50834C>A XP_016863882.1:n.-399-50834C>A
XM_017008394.1:c.-399-50834C>A XP_016863883.1:n.-399-50834C>A
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