Linked Data
dbSNP Id:
rs2151077199
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6181942C>A , CM000668.2:g.6181942C>A | GRCh38 |
| NC_000006.11:g.6182175C>A , CM000668.1:g.6182175C>A | GRCh37 |
| NC_000006.10:g.6127174C>A | NCBI36 |
| NG_008107.1:g.143750G>T , LRG_549:g.143750G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.1459+46G>T MANE Select | ENSP00000264870.3:n.1459+46G>T | |
| ENST00000264870.7:c.1459+46G>T | ENSP00000264870.3:n.1459+46G>T | |
| NM_000129.3:c.1459+46G>T , LRG_549t1:c.1459+46G>T | NP_000120.2:n.1459+46G>T | |
| XM_006715010.2:c.1459+46G>T | XP_006715073.1:n.1459+46G>T | |
| XM_011514342.1:c.1621+46G>T | XP_011512644.1:n.1621+46G>T | |
| NM_000129.4:c.1459+46G>T MANE Select | NP_000120.2:n.1459+46G>T |