Linked Data
dbSNP Id:
rs940497259
gnomAD v2:
5-148406064-T-C
gnomAD v3:
5-149026501-T-C
gnomAD v4:
5-149026501-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149026501T>C , CM000667.2:g.149026501T>C | GRCh38 |
| NC_000005.9:g.148406064T>C , CM000667.1:g.148406064T>C | GRCh37 |
| NC_000005.8:g.148386257T>C | NCBI36 |
| NG_007947.2:g.41674A>G , LRG_269:g.41674A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502274.2:c.2949+71A>G | ||
| ENST00000515425.6:c.3053+71A>G MANE Select | ENSP00000423660.1:n.3053+71A>G | |
| ENST00000675793.1:c.*2337+71A>G | ENSP00000502039.1:n.*2337+71A>G | |
| ENST00000676056.1:c.*2563+71A>G | ENSP00000501827.1:n.*2563+71A>G | |
| ENST00000323829.9:c.*2441+71A>G | ENSP00000313025.5:n.*2441+71A>G | |
| ENST00000504517.5:c.2583+71A>G | ENSP00000421779.1:n.2583+71A>G | |
| ENST00000504690.5:c.3053+71A>G | ENSP00000425627.1:n.3053+71A>G | |
| ENST00000510779.1:c.2103+71A>G | ||
| ENST00000512049.5:c.3032+71A>G | ENSP00000421860.1:n.3032+71A>G | |
| ENST00000513604.5:c.*2619A>G | ENSP00000423111.1:n.*2619A>G | |
| ENST00000515425.5:c.3053+71A>G | ENSP00000423660.1:n.3053+71A>G | |
| NM_024577.3:c.3053+71A>G , LRG_269t1:c.3053+71A>G | NP_078853.2:n.3053+71A>G | |
| NM_024577.4:c.3053+71A>G MANE Select | NP_078853.2:n.3053+71A>G |