Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.133448519G= , CM000665.2:g.133448519G= | GRCh38 |
| NC_000003.11:g.133167363G= , CM000665.1:g.133167363G= | GRCh37 |
| NC_000003.10:g.134650053G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302334.3:c.603G= (BFSP2) MANE Select | ENSP00000304987.2:p.Ala201= | |
| ENST00000302334.2:c.603G= (BFSP2) | ENSP00000304987.2:p.Ala201= | |
| XR_241567.2:n.743+262C= (BFSP2-AS1) | ||
| XR_924501.1:n.743+262C= (BFSP2-AS1) | ||
| NR_135276.1:n.495+262C= (BFSP2-AS1) | ||
| NR_135277.1:n.381-2944C= (BFSP2-AS1) | ||
| NR_135278.1:n.282+262C= (BFSP2-AS1) | ||
| XM_017007315.1:c.603G= (BFSP2) | XP_016862804.1:p.Ala201= | |
| XM_024453788.1:c.-58G= (BFSP2) | XP_024309556.1:n.-58G= | |
| NM_003571.4:c.603G= (BFSP2) MANE Select | NP_003562.1:p.Ala201= |