Linked Data
gnomAD v4:
2-135798096-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135798096C>G , CM000664.2:g.135798096C>G | GRCh38 |
| NC_000002.11:g.136555666C>G , CM000664.1:g.136555666C>G | GRCh37 |
| NC_000002.10:g.136272136C>G | NCBI36 |
| NG_008104.2:g.62074G>C , LRG_338:g.62074G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264162.7:c.4909G>C MANE Select | ENSP00000264162.2:p.Asp1637His | |
| ENST00000264162.6:c.4909G>C | ENSP00000264162.2:p.Asp1637His | |
| ENST00000452974.1:c.3002G>C | ENSP00000391231.1:p.Arg1001Thr | |
| NM_002299.2:c.4909G>C , LRG_338t1:c.4909G>C | NP_002290.2:p.Asp1637His | |
| NM_002299.3:c.4909G>C | NP_002290.2:p.Asp1637His | |
| XM_017004088.2:c.4909G>C | XP_016859577.1:p.Asp1637His | |
| NM_002299.4:c.4909G>C MANE Select | NP_002290.2:p.Asp1637His |