Linked Data
gnomAD v4:
22-39244616-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.39244616C>T , CM000684.2:g.39244616C>T | GRCh38 |
| NC_000022.10:g.39640621C>T , CM000684.1:g.39640621C>T | GRCh37 |
| NC_000022.9:g.37970567C>T | NCBI36 |
| NG_012111.1:g.5337G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331163.11:c.-653G>A MANE Select | ENSP00000330382.6:n.-653G>A | |
| ENST00000331163.10:c.-653G>A | ENSP00000330382.6:n.-653G>A | |
| NM_002608.2:c.-653G>A | NP_002599.1:n.-653G>A | |
| NM_002608.3:c.-653G>A | NP_002599.1:n.-653G>A | |
| NM_002608.4:c.-653G>A MANE Select | NP_002599.1:n.-653G>A |