MyVariant.info:
GRCh37
chr9:g.136132873T>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257486T>A , CM000671.2:g.133257486T>A | GRCh38 |
| NC_000009.11:g.136132873T>A , CM000671.1:g.136132873T>A | GRCh37 |
| NC_000009.10:g.135122694T>A | NCBI36 |
| NG_006669.1:g.20182A>T | |
| NG_006669.2:g.22730A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.326A>T | ||
| ENST00000647353.1:n.54-6334A>T | ||
| ENST00000651471.1:n.329+556A>T | ||
| ENST00000679909.1:c.28+17676A>T | ENSP00000506089.1:n.28+17676A>T | |
| ENST00000453660.3:n.308A>T | ||
| ENST00000538324.2:c.294A>T | ENSP00000483018.1:p.Thr98= | |
| ENST00000611156.4:c.294A>T | ENSP00000483265.1:p.Thr98= | |
| NM_020469.2:c.297A>T | NP_065202.2:p.Thr99= | |
| NM_020469.3:c.297A>T | NP_065202.2:p.Thr99= |