Linked Data
gnomAD v4:
9-129818714-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129818714C>T , CM000671.2:g.129818714C>T | GRCh38 |
| NC_000009.11:g.132580993C>T , CM000671.1:g.132580993C>T | GRCh37 |
| NC_000009.10:g.131620814C>T | NCBI36 |
| NG_008049.1:g.10449G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.620+31G>A MANE Select | ENSP00000345719.4:n.620+31G>A | |
| ENST00000651202.1:c.716+31G>A | ENSP00000498222.1:n.716+31G>A | |
| ENST00000351698.4:c.620+31G>A | ENSP00000345719.4:n.620+31G>A | |
| ENST00000473604.2:n.730+31G>A | ||
| ENST00000474192.1:n.37+31G>A | ||
| NM_000113.2:c.620+31G>A | NP_000104.1:n.620+31G>A | |
| XR_929731.1:n.780+31G>A | ||
| XR_929731.3:n.648+31G>A | ||
| NM_000113.3:c.620+31G>A MANE Select | NP_000104.1:n.620+31G>A |