MyVariant.info:
GRCh37
chr19:g.4117561C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4117563C>A , CM000681.2:g.4117563C>A | GRCh38 |
| NC_000019.9:g.4117561C>A , CM000681.1:g.4117561C>A | GRCh37 |
| NC_000019.8:g.4068561C>A | NCBI36 |
| NG_007996.1:g.11566G>T , LRG_750:g.11566G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394867.9:n.598G>T | ||
| ENST00000687128.1:n.598G>T | ||
| ENST00000262948.10:c.159G>T MANE Select | ENSP00000262948.4:p.Arg53= | |
| ENST00000262948.9:c.159G>T | ENSP00000262948.3:p.Arg53= | |
| ENST00000394867.8:c.-133G>T | ENSP00000378336.1:n.-133G>T | |
| ENST00000599345.1:n.356G>T | ||
| NM_030662.3:c.159G>T , LRG_750t1:c.159G>T | NP_109587.1:p.Arg53= | |
| XM_006722799.2:c.159G>T | XP_006722862.1:p.Arg53= | |
| XM_017026989.1:c.159G>T | XP_016882478.1:p.Arg53= | |
| XM_017026990.1:c.159G>T | XP_016882479.1:p.Arg53= | |
| XM_017026991.1:c.159G>T | XP_016882480.1:p.Arg53= | |
| NM_030662.4:c.159G>T MANE Select | NP_109587.1:p.Arg53= |