Linked Data
gnomAD v4:
19-39248136-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39248136C>A , CM000681.2:g.39248136C>A | GRCh38 |
| NC_000019.9:g.39738776C>A , CM000681.1:g.39738776C>A | GRCh37 |
| NC_000019.8:g.44430616C>A | NCBI36 |
| NG_042193.1:g.1836G>T | |
| NG_055295.1:g.5721G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000606380.2:c.152-141G>T | ENSP00000476098.1:n.152-141G>T | |
| ENST00000610963.1:c.151-141G>T | ENSP00000481371.1:n.151-141G>T | |
| ENST00000616270.4:c.152-141G>T | ENSP00000480679.1:n.152-141G>T | |
| ENST00000634680.1:c.151+293G>T | ENSP00000489240.1:n.151+293G>T | |
| ENST00000634967.1:c.152-141G>T | ENSP00000489559.1:n.152-141G>T | |
| NR_074079.1:n.429-141G>T |