Linked Data
gnomAD v4:
6-49451766-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49451766G>T , CM000668.2:g.49451766G>T | GRCh38 |
| NC_000006.11:g.49419479G>T , CM000668.1:g.49419479G>T | GRCh37 |
| NC_000006.10:g.49527438G>T | NCBI36 |
| NG_007100.1:g.16374C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.1084-52C>A MANE Select | ENSP00000274813.3:n.1084-52C>A | |
| ENST00000274813.3:c.1084-52C>A | ENSP00000274813.3:n.1084-52C>A | |
| NM_000255.3:c.1084-52C>A | NP_000246.2:n.1084-52C>A | |
| XM_005249143.2:c.1084-52C>A | XP_005249200.1:n.1084-52C>A | |
| XM_005249143.3:c.1084-52C>A | XP_005249200.1:n.1084-52C>A | |
| NM_000255.4:c.1084-52C>A MANE Select | NP_000246.2:n.1084-52C>A |