MyVariant.info:
GRCh37
chr5:g.160758058C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.161331051C>T , CM000667.2:g.161331051C>T | GRCh38 |
| NC_000005.9:g.160758058C>T , CM000667.1:g.160758058C>T | GRCh37 |
| NC_000005.8:g.160690636C>T | NCBI36 |
| NG_047050.1:g.222074G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274547.7:c.909G>A | ENSP00000274547.2:p.Lys303= | |
| ENST00000393959.6:c.909G>A MANE Select | ENSP00000377531.1:p.Lys303= | |
| ENST00000674514.1:n.991G>A | ||
| ENST00000675081.1:c.*368G>A | ENSP00000502207.1:n.*368G>A | |
| ENST00000675303.1:c.909G>A | ENSP00000502748.1:p.Lys303= | |
| ENST00000675381.1:c.657G>A | ENSP00000501968.1:p.Lys219= | |
| ENST00000675746.1:c.159G>A | ENSP00000502391.1:p.Lys53= | |
| ENST00000675773.1:c.909G>A | ENSP00000502701.1:p.Lys303= | |
| ENST00000274547.6:c.909G>A | ENSP00000274547.2:p.Lys303= | |
| ENST00000353437.10:c.909G>A | ENSP00000274546.6:p.Lys303= | |
| ENST00000393959.5:c.909G>A | ENSP00000377531.1:p.Lys303= | |
| ENST00000517547.5:c.429G>A | ENSP00000429750.1:p.Lys143= | |
| ENST00000517901.5:c.720G>A | ENSP00000430532.1:p.Lys240= | |
| ENST00000520240.5:c.909G>A | ENSP00000429320.1:p.Lys303= | |
| ENST00000612710.1:c.720G>A | ENSP00000480066.1:p.Lys240= | |
| NM_000813.2:c.909G>A | NP_000804.1:p.Lys303= | |
| NM_021911.2:c.909G>A | NP_068711.1:p.Lys303= | |
| XM_011534501.1:c.159G>A | XP_011532803.1:p.Lys53= | |
| NM_000813.3:c.909G>A | NP_000804.1:p.Lys303= | |
| NM_001371727.1:c.909G>A MANE Select | NP_001358656.1:p.Lys303= | |
| NM_021911.3:c.909G>A | NP_068711.1:p.Lys303= |