MyVariant.info:
GRCh37
chr22:g.36684331C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36288285C>A , CM000684.2:g.36288285C>A | GRCh38 |
| NC_000022.10:g.36684331C>A , CM000684.1:g.36684331C>A | GRCh37 |
| NC_000022.9:g.35014277C>A | NCBI36 |
| NG_011884.2:g.104734G>T , LRG_567:g.104734G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685801.1:c.4962G>T | ENSP00000510688.1:p.Arg1654= | |
| ENST00000691109.1:n.5194G>T | ||
| ENST00000216181.11:c.4899G>T MANE Select | ENSP00000216181.6:p.Arg1633= | |
| ENST00000216181.9:c.4899G>T | ENSP00000216181.5:p.Arg1633= | |
| NM_002473.5:c.4899G>T , LRG_567t1:c.4899G>T | NP_002464.1:p.Arg1633= | |
| XM_011530197.1:c.4899G>T | XP_011528499.1:p.Arg1633= | |
| XM_011530197.2:c.4899G>T | XP_011528499.1:p.Arg1633= | |
| XM_017028803.1:c.4899G>T | XP_016884292.1:p.Arg1633= | |
| XM_017028804.1:c.4899G>T | XP_016884293.1:p.Arg1633= | |
| XM_017028805.1:c.4899G>T | XP_016884294.1:p.Arg1633= | |
| XM_017028806.1:c.4899G>T | XP_016884295.1:p.Arg1633= | |
| NM_002473.6:c.4899G>T MANE Select | NP_002464.1:p.Arg1633= |