Linked Data
dbSNP Id:
rs1179439664
gnomAD v4:
9-127813355-C-T
MyVariant Identifiers:
chr9:g.130575634C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127813355C>T , CM000671.2:g.127813355C>T | GRCh38 |
| NC_000009.11:g.130575634C>T , CM000671.1:g.130575634C>T | GRCh37 |
| NC_000009.10:g.129615455C>T | NCBI36 |
| NG_009551.1:g.46414G>A , LRG_589:g.46414G>A | |
| NG_023245.1:g.15481C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373247.7:c.1515C>T MANE Select | ENSP00000362344.2:p.His505= | |
| ENST00000373225.7:c.1365C>T | ENSP00000362322.3:p.His455= | |
| ENST00000373228.5:c.*172C>T | ENSP00000362325.1:n.*172C>T | |
| ENST00000373247.6:c.1515C>T | ENSP00000362344.2:p.His505= | |
| ENST00000393706.6:c.1437C>T | ENSP00000377309.2:p.His479= | |
| ENST00000460181.5:n.1503C>T | ||
| ENST00000467826.5:n.709+32C>T | ||
| ENST00000475270.1:n.341C>T | ||
| ENST00000630236.2:c.*239C>T | ENSP00000486766.1:n.*239C>T | |
| NM_001018078.2:c.1365C>T | NP_001018088.1:p.His455= | |
| NM_001288803.1:c.1437C>T | NP_001275732.1:p.His479= | |
| NM_004957.5:c.1515C>T | NP_004948.4:p.His505= | |
| NR_110170.1:n.1563C>T | ||
| XM_005251864.2:c.1483+32C>T | XP_005251921.1:n.1483+32C>T | |
| XM_011518437.1:c.1365C>T | XP_011516739.1:p.His455= | |
| XM_011518438.1:c.1365C>T | XP_011516740.1:p.His455= | |
| XM_011518439.1:c.672C>T | XP_011516741.1:p.His224= | |
| XR_242581.2:n.1412C>T | ||
| XR_242582.2:n.1380+32C>T | ||
| XM_005251864.4:c.1483+32C>T | XP_005251921.1:n.1483+32C>T | |
| XM_011518439.2:c.672C>T | XP_011516741.1:p.His224= | |
| XM_017014565.2:c.1333+32C>T | XP_016870054.1:n.1333+32C>T | |
| XM_017014566.1:c.672C>T | XP_016870055.1:p.His224= | |
| XR_242581.4:n.1410C>T | ||
| XR_242582.4:n.1378+32C>T | ||
| NM_004957.6:c.1515C>T MANE Select | NP_004948.4:p.His505= |