HGVS | Genome Assembly |
---|---|
NC_000009.12:g.92718913G>T , CM000671.2:g.92718913G>T | GRCh38 |
NC_000009.11:g.95481195G>T , CM000671.1:g.95481195G>T | GRCh37 |
NC_000009.10:g.94521016G>T | NCBI36 |
NG_033908.1:g.50889C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000356884.11:c.1732C>A MANE Select | ENSP00000349351.6:p.Arg578Ser | |
ENST00000356884.10:c.1732C>A | ENSP00000349351.6:p.Arg578Ser | |
ENST00000375512.3:c.1732C>A | ENSP00000364662.3:p.Arg578Ser | |
NM_001003800.1:c.1732C>A | NP_001003800.1:p.Arg578Ser | |
NM_015250.3:c.1732C>A | NP_056065.1:p.Arg578Ser | |
XM_017014551.1:c.1813C>A | XP_016870040.1:p.Arg605Ser | |
NM_001003800.2:c.1732C>A MANE Select | NP_001003800.1:p.Arg578Ser | |
NM_015250.4:c.1732C>A | NP_056065.1:p.Arg578Ser |