Linked Data
dbSNP Id:
rs889899364
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119413718G>C , CM000665.2:g.119413718G>C | GRCh38 |
| NC_000003.11:g.119132565G>C , CM000665.1:g.119132565G>C | GRCh37 |
| NC_000003.10:g.120615255G>C | NCBI36 |
| NG_007665.2:g.124346G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.1927-138G>C MANE Select | ENSP00000264245.4:n.1927-138G>C | |
| ENST00000264245.8:c.1927-138G>C | ENSP00000264245.4:n.1927-138G>C | |
| NM_020754.3:c.1927-138G>C | NP_065805.2:n.1927-138G>C | |
| XM_005247671.3:c.1834-138G>C | XP_005247728.1:n.1834-138G>C | |
| XM_006713714.2:c.1867-138G>C | XP_006713777.1:n.1867-138G>C | |
| XM_006713714.3:c.1867-138G>C | XP_006713777.1:n.1867-138G>C | |
| XM_017006955.1:c.1435-138G>C | XP_016862444.1:n.1435-138G>C | |
| NM_020754.4:c.1927-138G>C MANE Select | NP_065805.2:n.1927-138G>C |