Linked Data
gnomAD v4:
19-44909394-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44909394T>C , CM000681.2:g.44909394T>C | GRCh38 |
| NC_000019.9:g.45412651T>C , CM000681.1:g.45412651T>C | GRCh37 |
| NC_000019.8:g.50104491T>C | NCBI36 |
| NG_007084.2:g.8613T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_000041.3:c.*144T>C | NP_000032.1:n.*144T>C | |
| NM_001302688.1:c.*144T>C | NP_001289617.1:n.*144T>C | |
| NM_001302689.1:c.*144T>C | NP_001289618.1:n.*144T>C | |
| NM_001302690.1:c.*144T>C | NP_001289619.1:n.*144T>C | |
| NM_001302691.1:c.*144T>C | NP_001289620.1:n.*144T>C |