Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.78874499C>A , CM000679.2:g.78874499C>A | GRCh38 |
| NC_000017.10:g.76870581C>A , CM000679.1:g.76870581C>A | GRCh37 |
| NC_000017.9:g.74382176C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000586713.6:c.-101-580G>T (TIMP2) | ENSP00000465968.2:n.-101-580G>T | |
| ENST00000262768.11:c.131-580G>T (TIMP2) MANE Select | ENSP00000262768.6:n.131-580G>T | |
| ENST00000536189.6:c.-101-580G>T (TIMP2) | ENSP00000441724.1:n.-101-580G>T | |
| ENST00000586713.5:c.-101-580G>T (CEP295NL) | ENSP00000465968.1:n.-101-580G>T | |
| NM_003255.4:c.131-580G>T (TIMP2) | NP_003246.1:n.131-580G>T | |
| NM_003255.5:c.131-580G>T (TIMP2) MANE Select | NP_003246.1:n.131-580G>T |