Linked Data
ClinVar Variation Id:
454964
dbSNP Id:
rs199600077
ExAC:
19:48801336 C / T
gnomAD v2:
19-48801336-C-T
gnomAD v3:
19-48298079-C-T
gnomAD v4:
19-48298079-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48298079C>T , CM000681.2:g.48298079C>T | GRCh38 |
| NC_000019.9:g.48801336C>T , CM000681.1:g.48801336C>T | GRCh37 |
| NC_000019.8:g.53493148C>T | NCBI36 |
| NG_033251.1:g.26997G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474199.6:c.1423G>A | ENSP00000501357.1:p.Asp475Asn | |
| ENST00000674207.1:c.*1112+98G>A | ENSP00000501374.1:n.*1112+98G>A | |
| ENST00000674294.1:c.1423G>A MANE Select | ENSP00000501363.1:p.Asp475Asn | |
| ENST00000315396.7:c.1312G>A | ENSP00000318429.7:p.Asp438Asn | |
| ENST00000474199.5:n.1440G>A | ||
| ENST00000497273.1:n.839G>A | ||
| NM_144577.3:c.1312G>A | NP_653178.3:p.Asp438Asn | |
| XM_005259413.2:c.1423G>A | XP_005259470.1:p.Asp475Asn | |
| XM_005259414.2:c.1423G>A | XP_005259471.1:p.Asp475Asn | |
| XM_005259415.2:c.1423G>A | XP_005259472.1:p.Asp475Asn | |
| XM_005259416.3:c.739G>A | XP_005259473.1:p.Asp247Asn | |
| XM_011527515.1:c.1312G>A | XP_011525817.1:p.Asp438Asn | |
| XM_011527516.1:c.1312G>A | XP_011525818.1:p.Asp438Asn | |
| NM_001364171.1:c.1423G>A | NP_001351100.1:p.Asp475Asn | |
| NM_144577.4:c.1312G>A | NP_653178.3:p.Asp438Asn | |
| XM_005259414.3:c.1423G>A | XP_005259471.1:p.Asp475Asn | |
| XM_005259415.3:c.1423G>A | XP_005259472.1:p.Asp475Asn | |
| XM_005259416.4:c.739G>A | XP_005259473.1:p.Asp247Asn | |
| XM_011527515.2:c.1312G>A | XP_011525817.1:p.Asp438Asn | |
| XM_011527516.2:c.1312G>A | XP_011525818.1:p.Asp438Asn | |
| XM_017027483.1:c.1147G>A | XP_016882972.1:p.Asp383Asn | |
| XM_024451782.1:c.1462G>A | XP_024307550.1:p.Asp488Asn | |
| XM_024451783.1:c.1423G>A | XP_024307551.1:p.Asp475Asn | |
| NM_001364171.2:c.1423G>A MANE Select | NP_001351100.1:p.Asp475Asn |