Linked Data
dbSNP Id:
rs1393095728
gnomAD v2:
2-241808584-C-G
gnomAD v3:
2-240869167-C-G
gnomAD v4:
2-240869167-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869167C>G , CM000664.2:g.240869167C>G | GRCh38 |
| NC_000002.11:g.241808584C>G , CM000664.1:g.241808584C>G | GRCh37 |
| NC_000002.10:g.241457257C>G | NCBI36 |
| NG_008005.1:g.5423C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.166-3C>G MANE Select | ENSP00000302620.3:n.166-3C>G | |
| ENST00000307503.3:c.166-3C>G | ENSP00000302620.3:n.166-3C>G | |
| ENST00000472436.1:n.186-3C>G | ||
| NM_000030.2:c.166-3C>G | NP_000021.1:n.166-3C>G | |
| XR_924060.1:n.405+1066G>C | ||
| NM_000030.3:c.166-3C>G MANE Select | NP_000021.1:n.166-3C>G |