HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154896215T>C , CM000685.2:g.154896215T>C | GRCh38 |
NC_000023.10:g.154124490T>C , CM000685.1:g.154124490T>C | GRCh37 |
NC_000023.9:g.153777684T>C | NCBI36 |
NG_011403.1:g.131509A>G | |
NG_011403.2:g.131509A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.6291A>G MANE Select | ENSP00000353393.4:p.Pro2097= | |
ENST00000360256.8:c.6291A>G | ENSP00000353393.4:p.Pro2097= | |
NM_000132.3:c.6291A>G | NP_000123.1:p.Pro2097= | |
XM_011531126.1:c.6186A>G | XP_011529428.1:p.Pro2062= | |
NM_000132.4:c.6291A>G MANE Select | NP_000123.1:p.Pro2097= |