Linked Data
dbSNP Id:
rs755864188
ExAC:
19:7593959 G / A
gnomAD v2:
19-7593959-G-A
gnomAD v3:
19-7529073-G-A
gnomAD v4:
19-7529073-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7529073G>A , CM000681.2:g.7529073G>A | GRCh38 |
| NC_000019.9:g.7593959G>A , CM000681.1:g.7593959G>A | GRCh37 |
| NC_000019.8:g.7499959G>A | NCBI36 |
| NG_015806.1:g.11464G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264079.11:c.1135-28G>A MANE Select | ENSP00000264079.5:n.1135-28G>A | |
| ENST00000264079.10:c.1135-28G>A | ENSP00000264079.5:n.1135-28G>A | |
| ENST00000394321.9:n.1450-28G>A | ||
| ENST00000594692.1:n.103G>A | ||
| ENST00000595860.5:n.318-28G>A | ||
| ENST00000599334.1:c.12-28G>A | ||
| NM_020533.2:c.1135-28G>A | NP_065394.1:n.1135-28G>A | |
| NM_020533.3:c.1135-28G>A MANE Select | NP_065394.1:n.1135-28G>A |