Linked Data
gnomAD v4:
2-72891699-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.72891699G>C , CM000664.2:g.72891699G>C | GRCh38 |
| NC_000002.11:g.73118828G>C , CM000664.1:g.73118828G>C | GRCh37 |
| NC_000002.10:g.72972336G>C | NCBI36 |
| NG_008234.1:g.9317G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000234454.6:c.*162G>C MANE Select | ENSP00000234454.5:n.*162G>C | |
| ENST00000234454.5:c.*162G>C | ENSP00000234454.5:n.*162G>C | |
| ENST00000498749.1:n.893G>C | ||
| NM_003124.4:c.*162G>C | NP_003115.1:n.*162G>C | |
| NM_003124.5:c.*162G>C MANE Select | NP_003115.1:n.*162G>C |