Linked Data
dbSNP Id:
rs1755020721
gnomAD v3:
5-149977898-A-T
gnomAD v4:
5-149977898-A-T
MyVariant Identifiers:
chr5:g.149357461A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149977898A>T , CM000667.2:g.149977898A>T | GRCh38 |
| NC_000005.9:g.149357461A>T , CM000667.1:g.149357461A>T | GRCh37 |
| NC_000005.8:g.149337654A>T | NCBI36 |
| NG_007147.2:g.19016A>T , LRG_684:g.19016A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.478A>T | ||
| ENST00000286298.5:c.246A>T MANE Select | ENSP00000286298.4:p.Pro82= | |
| ENST00000286298.4:c.246A>T | ENSP00000286298.4:p.Pro82= | |
| NM_000112.3:c.246A>T , LRG_684t1:c.246A>T | NP_000103.2:p.Pro82= | |
| XM_017009191.2:c.246A>T | XP_016864680.1:p.Pro82= | |
| NM_000112.4:c.246A>T MANE Select | NP_000103.2:p.Pro82= |