Linked Data
ClinVar Variation Id:
1203248
ClinVar RCV Id:
RCV001569222
dbSNP Id:
rs151319255
ExAC:
6:33132638 G / A
gnomAD v2:
6-33132638-G-A
gnomAD v3:
6-33164861-G-A
gnomAD v4:
6-33164861-G-A
COSMIC:
COSM82078
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33164861G>A , CM000668.2:g.33164861G>A | GRCh38 |
| NC_000006.11:g.33132638G>A , CM000668.1:g.33132638G>A | GRCh37 |
| NC_000006.10:g.33240616G>A | NCBI36 |
| NG_011589.1:g.32608C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000683572.1:n.660C>T | ||
| ENST00000341947.7:c.4854C>T MANE Select | ENSP00000339915.2:p.Asp1618= | |
| ENST00000341947.6:c.4854C>T | ENSP00000339915.2:p.Asp1618= | |
| ENST00000361917.5:c.4533C>T | ENSP00000355123.1:p.Asp1511= | |
| ENST00000374708.8:c.4596C>T | ENSP00000363840.4:p.Asp1532= | |
| ENST00000477772.1:n.644C>T | ||
| NM_080679.2:c.4533C>T | NP_542410.2:p.Asp1511= | |
| NM_080680.2:c.4854C>T | NP_542411.2:p.Asp1618= | |
| NM_080681.2:c.4596C>T | NP_542412.2:p.Asp1532= | |
| XM_011514298.1:c.4008C>T | XP_011512600.1:p.Asp1336= | |
| XM_011514299.1:c.4140C>T | XP_011512601.1:p.Asp1380= | |
| XM_011514300.1:c.3960C>T | XP_011512602.1:p.Asp1320= | |
| XM_011514301.1:c.3897C>T | XP_011512603.1:p.Asp1299= | |
| XM_011514302.1:c.3741C>T | XP_011512604.1:p.Asp1247= | |
| XM_011514299.2:c.4140C>T | XP_011512601.1:p.Asp1380= | |
| XM_011514300.2:c.3960C>T | XP_011512602.1:p.Asp1320= | |
| XM_011514302.2:c.3741C>T | XP_011512604.1:p.Asp1247= | |
| XM_017010250.1:c.4854C>T | XP_016865739.1:p.Asp1618= | |
| XM_017010251.2:c.3672C>T | XP_016865740.1:p.Asp1224= | |
| NM_080680.3:c.4854C>T MANE Select | NP_542411.2:p.Asp1618= | |
| NM_080681.3:c.4596C>T | NP_542412.2:p.Asp1532= | |
| NM_080679.3:c.4533C>T | NP_542410.2:p.Asp1511= |