Linked Data
dbSNP Id:
rs12494658
gnomAD v2:
3-85874476-T-C
gnomAD v3:
3-85825326-T-C
gnomAD v4:
3-85825326-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.85825326T>C , CM000665.2:g.85825326T>C | GRCh38 |
| NC_000003.11:g.85874476T>C , CM000665.1:g.85874476T>C | GRCh37 |
| NC_000003.10:g.85957166T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000383699.8:c.238+23130T>C (CADM2) MANE Select | ENSP00000373200.3:n.238+23130T>C | |
| ENST00000383699.7:c.238+23130T>C (CADM2) | ENSP00000373200.3:n.238+23130T>C | |
| ENST00000405615.2:c.217+23130T>C (CADM2) | ENSP00000384193.2:n.217+23130T>C | |
| ENST00000407528.6:c.211+23130T>C (CADM2) | ENSP00000384575.2:n.211+23130T>C | |
| NM_001167674.1:c.211+23130T>C (CADM2) | NP_001161146.1:n.211+23130T>C | |
| NM_001167675.1:c.238+23130T>C (CADM2) | NP_001161147.1:n.238+23130T>C | |
| NM_001256502.1:c.-114+23130T>C (CADM2) | NP_001243431.1:n.-114+23130T>C | |
| NM_001256503.1:c.-113-57965T>C (CADM2) | NP_001243432.1:n.-113-57965T>C | |
| NM_001256504.1:c.-114+23130T>C (CADM2) | NP_001243433.1:n.-114+23130T>C | |
| NM_001256505.1:c.-114+23130T>C (CADM2) | NP_001243434.1:n.-114+23130T>C | |
| NM_153184.3:c.217+23130T>C (CADM2) | NP_694854.2:n.217+23130T>C | |
| NR_046752.1:n.50+2675A>G (CADM2-AS2) | ||
| XM_006713081.2:c.211+23130T>C (CADM2) | XP_006713144.1:n.211+23130T>C | |
| XM_006713082.2:c.211+23130T>C (CADM2) | XP_006713145.1:n.211+23130T>C | |
| XM_006713081.4:c.211+23130T>C (CADM2) | XP_006713144.1:n.211+23130T>C | |
| XM_006713082.3:c.211+23130T>C (CADM2) | XP_006713145.1:n.211+23130T>C | |
| XM_017006062.2:c.253+23130T>C (CADM2) | XP_016861551.1:n.253+23130T>C | |
| XM_017006063.2:c.217+23130T>C (CADM2) | XP_016861552.1:n.217+23130T>C | |
| NM_001167674.2:c.211+23130T>C (CADM2) | NP_001161146.1:n.211+23130T>C | |
| NM_001167675.2:c.238+23130T>C (CADM2) MANE Select | NP_001161147.1:n.238+23130T>C | |
| NM_001256502.2:c.-114+23130T>C (CADM2) | NP_001243431.1:n.-114+23130T>C | |
| NM_001256503.2:c.-113-57965T>C (CADM2) | NP_001243432.1:n.-113-57965T>C | |
| NM_001256504.2:c.-114+23130T>C (CADM2) | NP_001243433.1:n.-114+23130T>C | |
| NM_001256505.2:c.-114+23130T>C (CADM2) | NP_001243434.1:n.-114+23130T>C | |
| NM_001375960.1:c.238+23130T>C (CADM2) | NP_001362889.1:n.238+23130T>C | |
| NM_001375961.1:c.190+23130T>C (CADM2) | NP_001362890.1:n.190+23130T>C | |
| NM_001375964.1:c.238+23130T>C (CADM2) | NP_001362893.1:n.238+23130T>C | |
| NM_001375967.1:c.89-57965T>C (CADM2) | NP_001362896.1:n.89-57965T>C | |
| NM_001375968.1:c.238+23130T>C (CADM2) | NP_001362897.1:n.238+23130T>C | |
| NM_153184.4:c.217+23130T>C (CADM2) | NP_694854.2:n.217+23130T>C | |
| NM_001381963.1:c.211+23130T>C (CADM2) | NP_001368892.1:n.211+23130T>C | |
| NM_001381964.1:c.211+23130T>C (CADM2) | NP_001368893.1:n.211+23130T>C |