Linked Data
gnomAD v4:
3-52224371-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52224371C>T , CM000665.2:g.52224371C>T | GRCh38 |
| NC_000003.11:g.52258387C>T , CM000665.1:g.52258387C>T | GRCh37 |
| NC_000003.10:g.52233427C>T | NCBI36 |
| NG_033933.1:g.6793G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360658.3:c.4-59G>A MANE Select | ENSP00000353874.2:n.4-59G>A | |
| ENST00000360658.2:c.4-59G>A | ENSP00000353874.2:n.4-59G>A | |
| ENST00000478201.1:c.223-104G>A | ||
| ENST00000494383.1:c.464-59G>A | ||
| NM_017442.3:c.4-59G>A | NP_059138.1:n.4-59G>A | |
| NM_017442.4:c.4-59G>A MANE Select | NP_059138.1:n.4-59G>A |