HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136046319T>C , CM000667.2:g.136046319T>C | GRCh38 |
NC_000005.9:g.135382008T>C , CM000667.1:g.135382008T>C | GRCh37 |
NC_000005.8:g.135409907T>C | NCBI36 |
NG_012646.1:g.22425T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000442011.7:c.299-16T>C MANE Select | ENSP00000416330.2:n.299-16T>C | |
ENST00000442011.6:c.299-16T>C | ENSP00000416330.2:n.299-16T>C | |
ENST00000504185.5:n.456-16T>C | ||
ENST00000506699.5:n.364-16T>C | ||
ENST00000507018.5:c.216-16T>C | ||
ENST00000515433.1:n.575T>C | ||
NM_000358.2:c.299-16T>C | NP_000349.1:n.299-16T>C | |
NM_000358.3:c.299-16T>C MANE Select | NP_000349.1:n.299-16T>C |