Linked Data
ClinVar Variation Id:
500471
dbSNP Id:
rs1464741803
gnomAD v2:
6-137143929-C-T
gnomAD v3:
6-136822791-C-T
gnomAD v4:
6-136822791-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.136822791C>T , CM000668.2:g.136822791C>T | GRCh38 |
| NC_000006.11:g.137143929C>T , CM000668.1:g.137143929C>T | GRCh37 |
| NC_000006.10:g.137185622C>T | NCBI36 |
| NG_008462.1:g.5212C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318471.5:c.126C>T MANE Select | ENSP00000315680.3:p.Ile42= | |
| ENST00000541292.6:c.126C>T | ENSP00000441004.1:p.Ile42= | |
| ENST00000678593.1:c.126C>T | ENSP00000503841.1:p.Ile42= | |
| ENST00000318471.4:c.126C>T | ENSP00000315680.3:p.Ile42= | |
| ENST00000367756.8:c.126C>T | ENSP00000356730.4:p.Ile42= | |
| ENST00000541292.5:c.126C>T | ENSP00000441004.1:p.Ile42= | |
| NM_000288.3:c.126C>T | NP_000279.1:p.Ile42= | |
| XM_006715502.1:c.126C>T | XP_006715565.1:p.Ile42= | |
| XM_011535900.1:c.126C>T | XP_011534202.1:p.Ile42= | |
| XM_006715502.2:c.126C>T | XP_006715565.1:p.Ile42= | |
| XM_017010934.2:c.126C>T | XP_016866423.1:p.Ile42= | |
| NM_000288.4:c.126C>T MANE Select | NP_000279.1:p.Ile42= |