Linked Data
dbSNP Id:
rs1486198984
gnomAD v2:
9-104187897-C-T
gnomAD v3:
9-101425615-C-T
gnomAD v4:
9-101425615-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101425615C>T , CM000671.2:g.101425615C>T | GRCh38 |
| NC_000009.11:g.104187897C>T , CM000671.1:g.104187897C>T | GRCh37 |
| NC_000009.10:g.103227718C>T | NCBI36 |
| NG_012387.1:g.15166G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647789.2:c.637G>A MANE Select | ENSP00000497767.1:p.Val213Ile | |
| ENST00000648064.1:c.637G>A | ENSP00000497990.1:p.Val213Ile | |
| ENST00000648758.1:c.637G>A | ENSP00000497731.1:p.Val213Ile | |
| ENST00000649902.1:c.637G>A | ENSP00000497216.1:p.Val213Ile | |
| ENST00000374855.8:c.637G>A | ENSP00000363988.4:p.Val213Ile | |
| ENST00000468981.3:n.164G>A | ||
| ENST00000616752.1:c.637G>A | ENSP00000481363.1:p.Val213Ile | |
| NM_000035.3:c.637G>A | NP_000026.2:p.Val213Ile | |
| NM_000035.4:c.637G>A MANE Select | NP_000026.2:p.Val213Ile |