Linked Data
ClinVar Variation Id:
235136
ClinVar RCV Id:
RCV000223943
dbSNP Id:
rs876661405
PubMed:
PMID:25589040
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44704140G>A , CM000681.2:g.44704140G>A | GRCh38 |
| NC_000019.9:g.45207410G>A , CM000681.1:g.45207410G>A | GRCh37 |
| NC_000019.8:g.49899250G>A | NCBI36 |
| NG_032692.2:g.9990G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000587331.7:c.505G>A (CEACAM16) MANE Select | ENSP00000466561.1:p.Gly169Arg | |
| ENST00000405314.2:c.505G>A (CEACAM16) | ENSP00000385576.1:p.Gly169Arg | |
| ENST00000587331.5:c.505G>A (CEACAM16) | ENSP00000466561.1:p.Gly169Arg | |
| NM_001039213.3:c.505G>A (CEACAM16) | NP_001034302.2:p.Gly169Arg | |
| XM_011526951.1:c.505G>A (CEACAM16) | XP_011525253.1:p.Gly169Arg | |
| NM_001039213.4:c.505G>A (CEACAM16) MANE Select | NP_001034302.2:p.Gly169Arg | |
| XM_017026795.1:c.505G>A (CEACAM16) | XP_016882284.1:p.Gly169Arg | |
| XR_001753953.1:n.436-4963C>T (CEACAM16-AS1) | ||
| XR_001753954.1:n.373-4963C>T (CEACAM16-AS1) |