HGVS | Genome Assembly |
---|---|
NC_000019.10:g.3770676C>G , CM000681.2:g.3770676C>G | GRCh38 |
NC_000019.9:g.3770674C>G , CM000681.1:g.3770674C>G | GRCh37 |
NC_000019.8:g.3721674C>G | NCBI36 |
NG_011565.1:g.6546G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000555633.3:c.500G>C MANE Select | ENSP00000450456.3:p.Arg167Pro | |
ENST00000555633.2:c.500G>C | ENSP00000450456.2:p.Arg167Pro | |
ENST00000555978.5:c.500G>C | ENSP00000450687.2:p.Arg167Pro | |
NM_032753.3:c.500G>C | NP_116142.1:p.Arg167Pro | |
XM_005259662.1:c.638G>C | XP_005259719.1:p.Arg213Pro | |
NM_001319074.1:c.638G>C | NP_001306003.1:p.Arg213Pro | |
NM_001319074.4:c.500G>C MANE Select | NP_001306003.2:p.Arg167Pro | |
NM_032753.4:c.500G>C | NP_116142.1:p.Arg167Pro |