Linked Data
gnomAD v4:
4-67740192-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67740192G>T , CM000666.2:g.67740192G>T | GRCh38 |
| NC_000004.11:g.68605910G>T , CM000666.1:g.68605910G>T | GRCh37 |
| NC_000004.10:g.68288505G>T | NCBI36 |
| NG_009293.1:g.20895C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.*288C>A MANE Select | ENSP00000226413.5:n.*288C>A | |
| ENST00000226413.4:c.*288C>A | ENSP00000226413.4:n.*288C>A | |
| NM_000406.2:c.*288C>A | NP_000397.1:n.*288C>A | |
| NM_001012763.1:c.*397C>A | NP_001012781.1:n.*397C>A | |
| NM_000406.3:c.*288C>A MANE Select | NP_000397.1:n.*288C>A | |
| NM_001012763.2:c.*397C>A | NP_001012781.1:n.*397C>A |