Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837607T>C , CM000685.2:g.154837607T>C | GRCh38 |
| NC_000023.10:g.154065882T>C , CM000685.1:g.154065882T>C | GRCh37 |
| NC_000023.9:g.153719076T>C | NCBI36 |
| NG_011403.1:g.190117A>G | |
| NG_033065.1:g.2056A>G | |
| NG_011403.2:g.190117A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.7046A>G MANE Select | NP_000123.1:p.Asp2349Gly |
| ENST00000360256.9:c.7046A>G MANE Select | ENSP00000353393.4:p.Asp2349Gly |
| NM_000132.3:c.7046A>G | NP_000123.1:p.Asp2349Gly |
| NM_019863.2:c.641A>G | NP_063916.1:p.Asp214Gly |
| NM_019863.3:c.641A>G | NP_063916.1:p.Asp214Gly |
| ENST00000330287.10:c.641A>G | ENSP00000327895.6:p.Asp214Gly |
| ENST00000360256.8:c.7046A>G | ENSP00000353393.4:p.Asp2349Gly |
| ENST00000644698.1:c.779A>G | ENSP00000495706.1:p.Asp260Gly |
| XM_011531126.1:c.6941A>G | XP_011529428.1:p.Asp2314Gly |