MyVariant.info:
GRCh37
chr22:g.19752621C>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19765098C>G , CM000684.2:g.19765098C>G | GRCh38 |
| NC_000022.10:g.19752621C>G , CM000684.1:g.19752621C>G | GRCh37 |
| NC_000022.9:g.18132621C>G | NCBI36 |
| NG_009229.1:g.13396C>G , LRG_226:g.13396C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700274.1:c.378C>G | ENSP00000514909.1:p.Ala126= | |
| ENST00000649276.2:c.852C>G MANE Select | ENSP00000497003.1:p.Ala284= | |
| ENST00000329705.11:c.825C>G | ENSP00000331176.7:p.Ala275= | |
| ENST00000332710.8:c.825C>G | ENSP00000331791.4:p.Ala275= | |
| ENST00000359500.7:c.825C>G | ENSP00000352483.3:p.Ala275= | |
| ENST00000484336.1:n.20C>G | ||
| ENST00000621939.1:c.825C>G | ENSP00000477982.1:p.Ala275= | |
| NM_005992.1:c.825C>G | NP_005983.1:p.Ala275= | |
| NM_080646.1:c.825C>G | NP_542377.1:p.Ala275= | |
| NM_080647.1:c.825C>G , LRG_226t1:c.825C>G | NP_542378.1:p.Ala275= | |
| XM_006724312.1:c.825C>G | XP_006724375.1:p.Ala275= | |
| XM_011530351.1:c.852C>G | XP_011528653.1:p.Ala284= | |
| XM_006724312.2:c.825C>G | XP_006724375.1:p.Ala275= | |
| XM_017028925.1:c.975C>G | XP_016884414.1:p.Ala325= | |
| XM_017028926.1:c.825C>G | XP_016884415.1:p.Ala275= | |
| XM_017028927.1:c.126C>G | XP_016884416.1:p.Ala42= | |
| XM_017028928.1:c.975C>G | XP_016884417.1:p.Ala325= | |
| NM_001379200.1:c.852C>G MANE Select | NP_001366129.1:p.Ala284= | |
| NM_080646.2:c.825C>G | NP_542377.1:p.Ala275= |