Linked Data
gnomAD v4:
2-135788061-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135788061C>G , CM000664.2:g.135788061C>G | GRCh38 |
| NC_000002.11:g.136545631C>G , CM000664.1:g.136545631C>G | GRCh37 |
| NC_000002.10:g.136262101C>G | NCBI36 |
| NG_008104.2:g.72109G>C , LRG_338:g.72109G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264162.7:c.*263G>C MANE Select | ENSP00000264162.2:n.*263G>C | |
| ENST00000264162.6:c.*263G>C | ENSP00000264162.2:n.*263G>C | |
| NM_002299.2:c.*263G>C , LRG_338t1:c.*263G>C | NP_002290.2:n.*263G>C | |
| NM_002299.3:c.*263G>C | NP_002290.2:n.*263G>C | |
| NM_002299.4:c.*263G>C MANE Select | NP_002290.2:n.*263G>C |