Linked Data
gnomAD v4:
2-43838940-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43838940G>T , CM000664.2:g.43838940G>T | GRCh38 |
| NC_000002.11:g.44066079G>T , CM000664.1:g.44066079G>T | GRCh37 |
| NC_000002.10:g.43919583G>T | NCBI36 |
| NG_008883.1:g.4880C>A | |
| NG_008884.1:g.4977G>T | |
| NG_008884.2:g.11999G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643284.1:n.521-5567G>T | ||
| ENST00000644611.1:c.76-5567G>T | ENSP00000495423.1:n.76-5567G>T | |
| XM_011533029.1:c.76-5567G>T | XP_011531331.1:n.76-5567G>T | |
| XM_011533030.1:c.76-5567G>T | XP_011531332.1:n.76-5567G>T | |
| XM_011533031.1:c.-153-5567G>T | XP_011531333.1:n.-153-5567G>T | |
| XR_939707.1:n.566-5567G>T | ||
| XM_011533029.2:c.76-5567G>T | XP_011531331.1:n.76-5567G>T | |
| XM_011533030.2:c.76-5567G>T | XP_011531332.1:n.76-5567G>T | |
| XR_001738891.1:n.580-5567G>T | ||
| XR_939707.2:n.580-5567G>T |