Linked Data
gnomAD v4:
3-13854889-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.13854889G>T , CM000665.2:g.13854889G>T | GRCh38 |
| NC_000003.11:g.13896386G>T , CM000665.1:g.13896386G>T | GRCh37 |
| NC_000003.10:g.13871387G>T | NCBI36 |
| NG_008088.1:g.30233C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285018.5:c.299-86C>A MANE Select | ENSP00000285018.4:n.299-86C>A | |
| ENST00000285018.4:c.299-86C>A | ENSP00000285018.4:n.299-86C>A | |
| NM_004625.3:c.299-86C>A | NP_004616.2:n.299-86C>A | |
| XM_011534090.1:c.98-86C>A | XP_011532392.1:n.98-86C>A | |
| XM_011534091.1:c.98-86C>A | XP_011532393.1:n.98-86C>A | |
| XM_011534091.2:c.98-86C>A | XP_011532393.1:n.98-86C>A | |
| NM_004625.4:c.299-86C>A MANE Select | NP_004616.2:n.299-86C>A |