Linked Data
dbSNP Id:
rs761024265
ExAC:
1:173878773 A / G
gnomAD v2:
1-173878773-A-G
gnomAD v4:
1-173909635-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173909635A>G , CM000663.2:g.173909635A>G | GRCh38 |
| NC_000001.10:g.173878773A>G , CM000663.1:g.173878773A>G | GRCh37 |
| NC_000001.9:g.172145396A>G | NCBI36 |
| NG_012462.1:g.12744T>C , LRG_577:g.12744T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.1070T>C MANE Select | ENSP00000356671.3:p.Ile357Thr | |
| ENST00000367698.3:c.1070T>C | ENSP00000356671.3:p.Ile357Thr | |
| ENST00000617423.4:c.560-2142T>C | ENSP00000478688.1:n.560-2142T>C | |
| NM_000488.3:c.1070T>C , LRG_577t1:c.1070T>C | NP_000479.1:p.Ile357Thr | |
| XM_005245198.2:c.926T>C | XP_005245255.1:p.Ile309Thr | |
| NM_001365052.1:c.926T>C | NP_001351981.1:p.Ile309Thr | |
| NM_000488.4:c.1070T>C MANE Select | NP_000479.1:p.Ile357Thr | |
| NM_001365052.2:c.926T>C | NP_001351981.1:p.Ile309Thr | |
| NM_001386302.1:c.1193T>C | NP_001373231.1:p.Ile398Thr | |
| NM_001386303.1:c.1151T>C | NP_001373232.1:p.Ile384Thr | |
| NM_001386304.1:c.1049T>C | NP_001373233.1:p.Ile350Thr | |
| NM_001386305.1:c.1013T>C | NP_001373234.1:p.Ile338Thr | |
| NM_001386306.1:c.854T>C | NP_001373235.1:p.Ile285Thr |