Linked Data
dbSNP Id:
rs1205366306
gnomAD v2:
19-6713647-T-C
gnomAD v3:
19-6713636-T-C
gnomAD v4:
19-6713636-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713636T>C , CM000681.2:g.6713636T>C | GRCh38 |
| NC_000019.9:g.6713647T>C , CM000681.1:g.6713647T>C | GRCh37 |
| NC_000019.8:g.6664647T>C | NCBI36 |
| NG_009557.1:g.12016A>G , LRG_27:g.12016A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.651-127A>G | ENSP00000512083.1:n.651-127A>G | |
| ENST00000245907.11:c.774-127A>G MANE Select | ENSP00000245907.4:n.774-127A>G | |
| ENST00000245907.10:c.774-127A>G | ENSP00000245907.4:n.774-127A>G | |
| ENST00000595577.1:n.278-127A>G | ||
| ENST00000597442.5:n.24-127A>G | ||
| NM_000064.3:c.774-127A>G | NP_000055.2:n.774-127A>G | |
| NM_000064.4:c.774-127A>G MANE Select | NP_000055.2:n.774-127A>G |