HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154860457A>G , CM000685.2:g.154860457A>G | GRCh38 |
NC_000023.10:g.154088732A>G , CM000685.1:g.154088732A>G | GRCh37 |
NC_000023.9:g.153741926A>G | NCBI36 |
NG_011403.1:g.167267T>C | |
NG_011403.2:g.167267T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.6875T>C MANE Select | ENSP00000353393.4:p.Leu2292Pro | |
ENST00000644698.1:c.608T>C | ENSP00000495706.1:p.Leu203Pro | |
ENST00000330287.10:c.470T>C | ENSP00000327895.6:p.Leu157Pro | |
ENST00000360256.8:c.6875T>C | ENSP00000353393.4:p.Leu2292Pro | |
NM_000132.3:c.6875T>C | NP_000123.1:p.Leu2292Pro | |
NM_019863.2:c.470T>C | NP_063916.1:p.Leu157Pro | |
XM_011531126.1:c.6770T>C | XP_011529428.1:p.Leu2257Pro | |
NM_000132.4:c.6875T>C MANE Select | NP_000123.1:p.Leu2292Pro | |
NM_019863.3:c.470T>C | NP_063916.1:p.Leu157Pro |