Canonical Allele Identifier: CA13267651
Gene: CABCOCO1 HGNC NCBI

Linked Data

dbSNP Id: rs4590817
gnomAD v2: 10-63467553-G-C
gnomAD v3: 10-61707795-G-C
gnomAD v4: 10-61707795-G-C
MyVariant Identifiers: chr10:g.63467553G>C (hg19) chr10:g.61707795G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61707795G>C , CM000672.2:g.61707795G>C GRCh38
NC_000010.10:g.63467553G>C , CM000672.1:g.63467553G>C GRCh37
NC_000010.9:g.63137559G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000648843.3:c.552+17174G>C MANE Select ENSP00000496918.2:n.552+17174G>C
ENST00000330194.2:c.288+17174G>C ENSP00000328698.2:n.288+17174G>C
NM_173554.2:c.288+17174G>C NP_775825.1:n.288+17174G>C
XM_005269598.2:c.414+17174G>C XP_005269655.1:n.414+17174G>C
XM_005269599.3:c.414+17174G>C XP_005269656.1:n.414+17174G>C
XM_005269600.3:c.288+17174G>C XP_005269657.1:n.288+17174G>C
XM_006717690.2:c.552+17174G>C XP_006717753.1:n.552+17174G>C
NM_001366905.1:c.288+17174G>C NP_001353834.1:n.288+17174G>C
NM_001366906.1:c.552+17174G>C NP_001353835.1:n.552+17174G>C
NM_001366908.1:c.414+17174G>C NP_001353837.1:n.414+17174G>C
XM_005269598.3:c.414+17174G>C XP_005269655.1:n.414+17174G>C
NM_001366905.2:c.288+17174G>C NP_001353834.1:n.288+17174G>C
NM_001366906.2:c.552+17174G>C MANE Select NP_001353835.1:n.552+17174G>C
NM_001366908.2:c.414+17174G>C NP_001353837.1:n.414+17174G>C
NM_173554.3:c.288+17174G>C NP_775825.1:n.288+17174G>C
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