MyVariant.info:
GRCh37
chr9:g.139407501G>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136513049G>A , CM000671.2:g.136513049G>A | GRCh38 |
| NC_000009.11:g.139407501G>A , CM000671.1:g.139407501G>A | GRCh37 |
| NC_000009.10:g.138527322G>A | NCBI36 |
| NG_007458.1:g.37738C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645828.1:n.246C>T | ||
| ENST00000646957.2:n.62C>T | ||
| ENST00000651671.1:c.2439C>T MANE Select | ENSP00000498587.1:p.Tyr813= | |
| ENST00000679595.1:c.2439C>T | ENSP00000506241.1:p.Tyr813= | |
| ENST00000680133.1:c.2325C>T | ENSP00000505319.1:p.Tyr775= | |
| ENST00000680218.1:c.2439C>T | ENSP00000505339.1:p.Tyr813= | |
| ENST00000680668.1:c.2325C>T | ENSP00000506336.1:p.Tyr775= | |
| ENST00000680924.1:c.2439C>T | ENSP00000506031.1:p.Tyr813= | |
| ENST00000681135.1:c.2439C>T | ENSP00000506636.1:p.Tyr813= | |
| ENST00000681454.1:c.*1675C>T | ENSP00000505763.1:n.*1675C>T | |
| ENST00000277541.6:c.2439C>T | ENSP00000277541.6:p.Tyr813= | |
| NM_017617.3:c.2439C>T | NP_060087.3:p.Tyr813= | |
| XM_011518717.1:c.1740C>T | XP_011517019.1:p.Tyr580= | |
| NM_017617.5:c.2439C>T MANE Select | NP_060087.3:p.Tyr813= | |
| XM_011518717.2:c.1716C>T | XP_011517019.2:p.Tyr572= |