Linked Data
dbSNP Id:
rs1279368319
gnomAD v2:
11-102661683-T-C
gnomAD v3:
11-102790952-T-C
gnomAD v4:
11-102790952-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102790952T>C , CM000673.2:g.102790952T>C | GRCh38 |
| NC_000011.9:g.102661683T>C , CM000673.1:g.102661683T>C | GRCh37 |
| NC_000011.8:g.102166893T>C | NCBI36 |
| NG_011740.1:g.12284A>G | |
| NG_011740.2:g.12284A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000315274.7:c.1197-146A>G (MMP1) MANE Select | ENSP00000322788.6:n.1197-146A>G | |
| ENST00000680179.1:n.375-146A>G (MMP1) | ||
| ENST00000681445.1:n.371-146A>G (MMP1) | ||
| ENST00000681643.1:n.397-146A>G (MMP1) | ||
| ENST00000315274.6:c.1197-146A>G (MMP1) | ENSP00000322788.6:n.1197-146A>G | |
| ENST00000371455.7:n.325-7072T>C (WTAPP1) | ||
| ENST00000525739.6:n.390-2193T>C (WTAPP1) | ||
| ENST00000544704.1:n.344+6888T>C (WTAPP1) | ||
| NM_001145938.1:c.999-146A>G (MMP1) | NP_001139410.1:n.999-146A>G | |
| NM_002421.3:c.1197-146A>G (MMP1) | NP_002412.1:n.1197-146A>G | |
| NR_038390.1:n.390-2193T>C (WTAPP1) | ||
| NM_002421.4:c.1197-146A>G (MMP1) MANE Select | NP_002412.1:n.1197-146A>G | |
| NM_001145938.2:c.999-146A>G (MMP1) | NP_001139410.1:n.999-146A>G |