Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135808692G>C , CM000664.2:g.135808692G>C | GRCh38 |
| NC_000002.11:g.136566262G>C , CM000664.1:g.136566262G>C | GRCh37 |
| NC_000002.10:g.136282732G>C | NCBI36 |
| NG_008104.2:g.51478C>G , LRG_338:g.51478C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002299.4:c.3655C>G MANE Select | NP_002290.2:p.Pro1219Ala |
| ENST00000264162.7:c.3655C>G MANE Select | ENSP00000264162.2:p.Pro1219Ala |
| NM_002299.2:c.3655C>G , LRG_338t1:c.3655C>G | NP_002290.2:p.Pro1219Ala |
| NM_002299.3:c.3655C>G | NP_002290.2:p.Pro1219Ala |
| ENST00000264162.6:c.3655C>G | ENSP00000264162.2:p.Pro1219Ala |
| ENST00000452974.1:c.1951C>G | ENSP00000391231.1:p.Pro651Ala |
| XM_017004088.2:c.3655C>G | XP_016859577.1:p.Pro1219Ala |