Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816202A>G , CM000681.2:g.4816202A>G | GRCh38 |
| NC_000019.9:g.4816214A>G , CM000681.1:g.4816214A>G | GRCh37 |
| NC_000019.8:g.4767214A>G | NCBI36 |
| NG_031998.1:g.20541T>C , LRG_358:g.20541T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.*37T>C MANE Select | ENSP00000248244.4:n.*37T>C | |
| ENST00000248244.5:c.*37T>C | ENSP00000248244.4:n.*37T>C | |
| NM_182919.3:c.*37T>C , LRG_358t1:c.*37T>C | NP_891549.1:n.*37T>C | |
| NM_001385678.1:c.*37T>C | NP_001372607.1:n.*37T>C | |
| NM_001385679.1:c.*37T>C | NP_001372608.1:n.*37T>C | |
| NM_001385680.1:c.*37T>C | NP_001372609.1:n.*37T>C | |
| NM_182919.4:c.*37T>C MANE Select | NP_891549.1:n.*37T>C |