HGVS | Genome Assembly |
---|---|
NC_000009.12:g.92718853C>A , CM000671.2:g.92718853C>A | GRCh38 |
NC_000009.11:g.95481135C>A , CM000671.1:g.95481135C>A | GRCh37 |
NC_000009.10:g.94520956C>A | NCBI36 |
NG_033908.1:g.50949G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356884.11:c.1792G>T MANE Select | ENSP00000349351.6:p.Ala598Ser | |
ENST00000356884.10:c.1792G>T | ENSP00000349351.6:p.Ala598Ser | |
ENST00000375512.3:c.1792G>T | ENSP00000364662.3:p.Ala598Ser | |
NM_001003800.1:c.1792G>T | NP_001003800.1:p.Ala598Ser | |
NM_015250.3:c.1792G>T | NP_056065.1:p.Ala598Ser | |
XM_017014551.1:c.1873G>T | XP_016870040.1:p.Ala625Ser | |
NM_001003800.2:c.1792G>T MANE Select | NP_001003800.1:p.Ala598Ser | |
NM_015250.4:c.1792G>T | NP_056065.1:p.Ala598Ser |