HGVS | Genome Assembly |
---|---|
NC_000009.12:g.98542043G>A , CM000671.2:g.98542043G>A | GRCh38 |
NC_000009.11:g.101304325G>A , CM000671.1:g.101304325G>A | GRCh37 |
NC_000009.10:g.100344146G>A | NCBI36 |
NG_016426.1:g.172155C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259455.4:c.460C>T MANE Select | ENSP00000259455.2:p.Leu154Phe | |
ENST00000637410.1:n.238C>T | ||
ENST00000637717.1:c.76C>T | ENSP00000490789.1:p.Leu26Phe | |
ENST00000638001.1:n.70C>T | ||
ENST00000259455.3:c.460C>T | ENSP00000259455.2:p.Leu154Phe | |
ENST00000477471.1:n.247C>T | ||
ENST00000634227.1:n.234C>T | ||
NM_005458.7:c.460C>T | NP_005449.5:p.Leu154Phe | |
XM_017015331.2:c.166C>T | XP_016870820.1:p.Leu56Phe | |
NM_005458.8:c.460C>T MANE Select | NP_005449.5:p.Leu154Phe |