Linked Data
dbSNP Id:
rs747353119
gnomAD v4:
9-136497175-G-A
MyVariant Identifiers:
chr9:g.139391627G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136497175G>A , CM000671.2:g.136497175G>A | GRCh38 |
| NC_000009.11:g.139391627G>A , CM000671.1:g.139391627G>A | GRCh37 |
| NC_000009.10:g.138511448G>A | NCBI36 |
| NG_007458.1:g.53612C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651671.1:c.6564C>T MANE Select | ENSP00000498587.1:p.Gly2188= | |
| ENST00000679595.1:c.*1604C>T | ENSP00000506241.1:n.*1604C>T | |
| ENST00000679969.1:n.3160C>T | ||
| ENST00000680003.1:n.2896C>T | ||
| ENST00000680133.1:c.6450C>T | ENSP00000505319.1:p.Gly2150= | |
| ENST00000680218.1:c.6444C>T | ENSP00000505339.1:p.Gly2148= | |
| ENST00000680668.1:c.6450C>T | ENSP00000506336.1:p.Gly2150= | |
| ENST00000680778.1:c.4161C>T | ENSP00000506033.1:p.Gly1387= | |
| ENST00000680924.1:c.*3964C>T | ENSP00000506031.1:n.*3964C>T | |
| ENST00000681135.1:c.*4173C>T | ENSP00000506636.1:n.*4173C>T | |
| ENST00000681298.1:n.4669C>T | ||
| ENST00000681454.1:c.*5800C>T | ENSP00000505763.1:n.*5800C>T | |
| ENST00000277541.6:c.6564C>T | ENSP00000277541.6:p.Gly2188= | |
| NM_017617.3:c.6564C>T | NP_060087.3:p.Gly2188= | |
| XM_011518717.1:c.5865C>T | XP_011517019.1:p.Gly1955= | |
| NM_017617.5:c.6564C>T MANE Select | NP_060087.3:p.Gly2188= | |
| XM_011518717.2:c.5841C>T | XP_011517019.2:p.Gly1947= |