MyVariant.info:
GRCh38
chr3:g.11191093G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.11191093G>T , CM000665.2:g.11191093G>T | GRCh38 |
| NC_000003.11:g.11232779G>T , CM000665.1:g.11232779G>T | GRCh37 |
| NC_000003.10:g.11207779G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000431010.3:c.-36+36539G>T MANE Select | ENSP00000397028.2:n.-36+36539G>T | |
| ENST00000431010.2:c.-36+36539G>T | ENSP00000397028.2:n.-36+36539G>T | |
| ENST00000438284.2:c.-36+53694G>T | ENSP00000406705.2:n.-36+53694G>T | |
| NM_001098212.1:c.-36+36539G>T | NP_001091682.1:n.-36+36539G>T | |
| NM_001098213.1:c.-36+53694G>T | NP_001091683.1:n.-36+53694G>T | |
| XM_011533653.1:c.-36+35962G>T | XP_011531955.1:n.-36+35962G>T | |
| XM_011533653.2:c.-36+35962G>T | XP_011531955.1:n.-36+35962G>T | |
| XM_017006284.1:c.-36+35204G>T | XP_016861773.1:n.-36+35204G>T | |
| NM_001098212.2:c.-36+36539G>T MANE Select | NP_001091682.1:n.-36+36539G>T | |
| NM_001098213.2:c.-36+53694G>T | NP_001091683.1:n.-36+53694G>T |