MyVariant.info:
GRCh37
chr13:g.48955538C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48381402C>A , CM000675.2:g.48381402C>A | GRCh38 |
| NC_000013.10:g.48955538C>A , CM000675.1:g.48955538C>A | GRCh37 |
| NC_000013.9:g.47853539C>A | NCBI36 |
| NG_009009.1:g.82656C>A , LRG_517:g.82656C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.1654C>A MANE Select | ENSP00000267163.4:p.Arg552= | |
| ENST00000643064.1:c.153C>A | ||
| ENST00000650461.1:c.1654C>A | ENSP00000497193.1:p.Arg552= | |
| ENST00000267163.4:c.1654C>A | ENSP00000267163.4:p.Arg552= | |
| NM_000321.2:c.1654C>A , LRG_517t1:c.1654C>A | NP_000312.2:p.Arg552= | |
| XM_011535171.1:c.1393C>A | XP_011533473.1:p.Arg465= | |
| XM_011535171.2:c.1393C>A | XP_011533473.1:p.Arg465= | |
| NM_000321.3:c.1654C>A MANE Select | NP_000312.2:p.Arg552= |