Linked Data
gnomAD v4:
17-4932436-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4932436G>A , CM000679.2:g.4932436G>A | GRCh38 |
| NC_000017.10:g.4835731G>A , CM000679.1:g.4835731G>A | GRCh37 |
| NC_000017.9:g.4776511G>A | NCBI36 |
| NG_008767.2:g.5142G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329125.6:c.-7+71G>A (GP1BA) MANE Select | ENSP00000329380.5:n.-7+71G>A | |
| ENST00000649830.1:c.-888+1906C>T (CHRNE) | ENSP00000496907.1:n.-888+1906C>T | |
| ENST00000329125.5:c.-7+71G>A (GP1BA) | ENSP00000329380.5:n.-7+71G>A | |
| ENST00000611961.1:c.-7+71G>A (GP1BA) | ENSP00000484439.1:n.-7+71G>A | |
| NM_000173.6:c.-7+71G>A (GP1BA) | NP_000164.5:n.-7+71G>A | |
| NM_000173.7:c.-7+71G>A (GP1BA) MANE Select | NP_000164.5:n.-7+71G>A |