Linked Data
dbSNP Id:
rs751465176
ExAC:
9:3856152 A / T
gnomAD v2:
9-3856152-A-T
gnomAD v4:
9-3856152-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.3856152A>T , CM000671.2:g.3856152A>T | GRCh38 |
| NC_000009.11:g.3856152A>T , CM000671.1:g.3856152A>T | GRCh37 |
| NC_000009.10:g.3846152A>T | NCBI36 |
| NG_011782.1:g.448884T>A | |
| NG_011782.2:g.448884T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000464391.2:n.888T>A | ||
| ENST00000491889.6:c.*1693T>A | ENSP00000419914.1:n.*1693T>A | |
| ENST00000645252.2:n.772T>A | ||
| ENST00000682749.1:c.1865T>A | ENSP00000507306.1:p.Ile622Asn | |
| ENST00000682846.1:c.132-26660T>A | ENSP00000507527.1:n.132-26660T>A | |
| ENST00000682864.1:n.829T>A | ||
| ENST00000381971.8:c.2330T>A MANE Select | ENSP00000371398.3:p.Ile777Asn | |
| ENST00000645252.1:n.772T>A | ||
| ENST00000324333.14:c.1865T>A | ENSP00000325494.10:p.Ile622Asn | |
| ENST00000381971.7:c.2330T>A | ENSP00000371398.3:p.Ile777Asn | |
| ENST00000461870.5:n.686T>A | ||
| ENST00000467497.6:n.870T>A | ||
| NM_001042413.1:c.2330T>A | NP_001035878.1:p.Ile777Asn | |
| NM_152629.3:c.1865T>A | NP_689842.3:p.Ile622Asn | |
| XM_005251386.3:c.1865T>A | XP_005251443.1:p.Ile622Asn | |
| XM_005251387.3:c.1664T>A | XP_005251444.1:p.Ile555Asn | |
| XM_005251388.3:c.1664T>A | XP_005251445.1:p.Ile555Asn | |
| XM_011517763.1:c.2330T>A | XP_011516065.1:p.Ile777Asn | |
| XM_011517764.1:c.2330T>A | XP_011516066.1:p.Ile777Asn | |
| XM_011517765.1:c.2330T>A | XP_011516067.1:p.Ile777Asn | |
| XM_011517766.1:c.1865T>A | XP_011516068.1:p.Ile622Asn | |
| XM_011517767.1:c.1664T>A | XP_011516069.1:p.Ile555Asn | |
| XM_005251386.4:c.1865T>A | XP_005251443.1:p.Ile622Asn | |
| XM_005251387.4:c.1664T>A | XP_005251444.1:p.Ile555Asn | |
| XM_005251388.4:c.1664T>A | XP_005251445.1:p.Ile555Asn | |
| XM_011517763.2:c.2330T>A | XP_011516065.1:p.Ile777Asn | |
| XM_011517764.2:c.2330T>A | XP_011516066.1:p.Ile777Asn | |
| XM_011517765.2:c.2330T>A | XP_011516067.1:p.Ile777Asn | |
| XM_011517766.2:c.1865T>A | XP_011516068.1:p.Ile622Asn | |
| XM_011517767.3:c.1664T>A | XP_011516069.1:p.Ile555Asn | |
| XM_017014361.1:c.1865T>A | XP_016869850.1:p.Ile622Asn | |
| NM_001042413.2:c.2330T>A MANE Select | NP_001035878.1:p.Ile777Asn | |
| NM_152629.4:c.1865T>A | NP_689842.3:p.Ile622Asn |