Linked Data
dbSNP Id:
rs2113815218
gnomAD v4:
5-150073369-G-A
MyVariant Identifiers:
chr5:g.149452932G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.150073369G>A , CM000667.2:g.150073369G>A | GRCh38 |
| NC_000005.9:g.149452932G>A , CM000667.1:g.149452932G>A | GRCh37 |
| NC_000005.8:g.149433125G>A | NCBI36 |
| NG_012303.1:g.45004C>T | |
| NG_012303.2:g.45004C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000675795.1:c.1014C>T MANE Select | ENSP00000501699.1:p.Tyr338= | |
| ENST00000286301.7:c.1014C>T | ENSP00000286301.3:p.Tyr338= | |
| ENST00000504875.5:c.1014C>T | ENSP00000422212.1:p.Tyr338= | |
| ENST00000543093.1:c.890-2798C>T | ENSP00000445282.1:n.890-2798C>T | |
| NM_001288705.1:c.1014C>T | NP_001275634.1:p.Tyr338= | |
| NM_005211.3:c.1014C>T | NP_005202.2:p.Tyr338= | |
| NR_109969.1:n.1227C>T | ||
| NM_001288705.2:c.1014C>T | NP_001275634.1:p.Tyr338= | |
| NM_001349736.1:c.1014C>T | NP_001336665.1:p.Tyr338= | |
| NM_001288705.3:c.1014C>T MANE Select | NP_001275634.1:p.Tyr338= | |
| NM_001375320.1:c.1014C>T | NP_001362249.1:p.Tyr338= | |
| NM_001375321.1:c.570C>T | NP_001362250.1:p.Tyr190= | |
| NR_164679.1:n.1070C>T | ||
| NM_001349736.2:c.1014C>T | NP_001336665.1:p.Tyr338= | |
| NM_005211.4:c.1014C>T | NP_005202.2:p.Tyr338= | |
| NR_109969.2:n.1141C>T |