Linked Data
dbSNP Id:
rs748905272
ExAC:
1:40558074 A / G
gnomAD v2:
1-40558074-A-G
gnomAD v4:
1-40092402-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40092402A>G , CM000663.2:g.40092402A>G | GRCh38 |
| NC_000001.10:g.40558074A>G , CM000663.1:g.40558074A>G | GRCh37 |
| NC_000001.9:g.40330661A>G | NCBI36 |
| NG_009192.1:g.10069T>C , LRG_690:g.10069T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372779.9:c.*66T>C | ENSP00000361865.5:n.*66T>C | |
| ENST00000433473.8:c.227T>C | ENSP00000394863.4:p.Met76Thr | |
| ENST00000439754.6:c.230T>C | ENSP00000403207.2:p.Met77Thr | |
| ENST00000449045.7:c.125-2890T>C | ENSP00000392293.2:n.125-2890T>C | |
| ENST00000526547.2:c.510T>C | ||
| ENST00000527311.7:c.230T>C | ENSP00000436695.3:p.Met77Thr | |
| ENST00000530704.6:c.230T>C | ENSP00000431655.1:p.Met77Thr | |
| ENST00000641083.1:c.208T>C | ||
| ENST00000641236.1:n.242T>C | ||
| ENST00000641319.1:c.230T>C | ENSP00000493128.1:p.Met77Thr | |
| ENST00000641471.1:c.317T>C | ENSP00000493146.1:p.Met106Thr | |
| ENST00000641548.1:c.*82T>C | ENSP00000492984.1:n.*82T>C | |
| ENST00000641691.1:c.*82T>C | ENSP00000492910.1:n.*82T>C | |
| ENST00000641924.1:c.124+4713T>C | ENSP00000493063.1:n.124+4713T>C | |
| ENST00000642050.2:c.230T>C MANE Select | ENSP00000493153.1:p.Met77Thr | |
| ENST00000372779.8:c.317T>C | ENSP00000361865.4:p.Met106Thr | |
| ENST00000433473.7:c.230T>C | ENSP00000394863.3:p.Met77Thr | |
| ENST00000449045.6:c.125-2890T>C | ENSP00000392293.2:n.125-2890T>C | |
| ENST00000526547.1:c.80T>C | ENSP00000436481.1:p.Met27Thr | |
| ENST00000527311.6:c.125-345T>C | ENSP00000436695.2:n.125-345T>C | |
| ENST00000529905.5:c.230T>C | ENSP00000432053.1:p.Met77Thr | |
| ENST00000530704.5:c.230T>C | ENSP00000431655.1:p.Met77Thr | |
| NM_000310.3:c.230T>C , LRG_690t1:c.230T>C | NP_000301.1:p.Met77Thr | |
| NM_001142604.1:c.125-2890T>C | NP_001136076.1:n.125-2890T>C | |
| XM_005271008.1:c.230T>C | XP_005271065.1:p.Met77Thr | |
| NM_001363695.1:c.230T>C | NP_001350624.1:p.Met77Thr | |
| NM_000310.4:c.230T>C MANE Select | NP_000301.1:p.Met77Thr | |
| NM_001142604.2:c.125-2890T>C | NP_001136076.1:n.125-2890T>C | |
| NM_001363695.2:c.230T>C | NP_001350624.1:p.Met77Thr |