Linked Data
gnomAD v4:
X-155259737-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155259737G>T , CM000685.2:g.155259737G>T | GRCh38 |
| NC_000023.10:g.154489022G>T , CM000685.1:g.154489022G>T | GRCh37 |
| NC_000023.9:g.154142216G>T | NCBI36 |
| NG_012626.2:g.9825C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369454.4:c.*1066C>A MANE Select | ENSP00000358466.3:n.*1066C>A | |
| ENST00000369454.3:c.*1066C>A | ENSP00000358466.3:n.*1066C>A | |
| NM_171998.3:c.*1066C>A | NP_741995.1:n.*1066C>A | |
| NM_171998.4:c.*1066C>A MANE Select | NP_741995.1:n.*1066C>A |