Linked Data
dbSNP Id:
rs747704954
ExAC:
4:122607560 T / C
gnomAD v2:
4-122607560-T-C
gnomAD v4:
4-121686405-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121686405T>C , CM000666.2:g.121686405T>C | GRCh38 |
| NC_000004.11:g.122607560T>C , CM000666.1:g.122607560T>C | GRCh37 |
| NC_000004.10:g.122827010T>C | NCBI36 |
| NG_032042.1:g.15588A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296511.10:c.10-33A>G MANE Select | ENSP00000296511.5:n.10-33A>G | |
| ENST00000296511.9:c.10-33A>G | ENSP00000296511.5:n.10-33A>G | |
| ENST00000501272.6:c.10-2928A>G | ENSP00000424106.1:n.10-2928A>G | |
| ENST00000506395.5:c.10-33A>G | ENSP00000421421.1:n.10-33A>G | |
| ENST00000509016.5:n.131-33A>G | ||
| ENST00000511552.5:n.396-33A>G | ||
| ENST00000513428.5:n.175-33A>G | ||
| ENST00000513523.1:n.178-33A>G | ||
| ENST00000513728.1:c.10-33A>G | ENSP00000427135.1:n.10-33A>G | |
| ENST00000515017.5:c.10-33A>G | ENSP00000424199.1:n.10-33A>G | |
| NM_001154.3:c.10-33A>G | NP_001145.1:n.10-33A>G | |
| XM_017008141.2:c.10-33A>G | XP_016863630.1:n.10-33A>G | |
| NM_001154.4:c.10-33A>G MANE Select | NP_001145.1:n.10-33A>G |