Linked Data
dbSNP Id:
rs1299623054
gnomAD v2:
19-7125648-T-C
gnomAD v3:
19-7125637-T-C
gnomAD v4:
19-7125637-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7125637T>C , CM000681.2:g.7125637T>C | GRCh38 |
| NC_000019.9:g.7125648T>C , CM000681.1:g.7125648T>C | GRCh37 |
| NC_000019.8:g.7076648T>C | NCBI36 |
| NG_008852.2:g.173364A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302850.10:c.3014-110A>G MANE Select | ENSP00000303830.4:n.3014-110A>G | |
| ENST00000302850.9:c.3014-110A>G | ENSP00000303830.4:n.3014-110A>G | |
| ENST00000341500.9:c.2978-110A>G | ENSP00000342838.4:n.2978-110A>G | |
| NM_000208.2:c.3014-110A>G | NP_000199.2:n.3014-110A>G | |
| NM_000208.3:c.3014-110A>G | NP_000199.2:n.3014-110A>G | |
| NM_001079817.1:c.2978-110A>G | NP_001073285.1:n.2978-110A>G | |
| NM_001079817.2:c.2978-110A>G | NP_001073285.1:n.2978-110A>G | |
| XM_011527988.1:c.3089-110A>G | XP_011526290.1:n.3089-110A>G | |
| XM_011527989.1:c.3053-110A>G | XP_011526291.1:n.3053-110A>G | |
| XM_011527988.2:c.3011-110A>G | XP_011526290.2:n.3011-110A>G | |
| XM_011527989.3:c.2975-110A>G | XP_011526291.2:n.2975-110A>G | |
| NM_000208.4:c.3014-110A>G MANE Select | NP_000199.2:n.3014-110A>G | |
| NM_001079817.3:c.2978-110A>G | NP_001073285.1:n.2978-110A>G |