HGVS | Genome Assembly |
---|---|
NC_000009.12:g.92718816C>G , CM000671.2:g.92718816C>G | GRCh38 |
NC_000009.11:g.95481098C>G , CM000671.1:g.95481098C>G | GRCh37 |
NC_000009.10:g.94520919C>G | NCBI36 |
NG_033908.1:g.50986G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356884.11:c.1829G>C MANE Select | ENSP00000349351.6:p.Gly610Ala | |
ENST00000356884.10:c.1829G>C | ENSP00000349351.6:p.Gly610Ala | |
ENST00000375512.3:c.1829G>C | ENSP00000364662.3:p.Gly610Ala | |
NM_001003800.1:c.1829G>C | NP_001003800.1:p.Gly610Ala | |
NM_015250.3:c.1829G>C | NP_056065.1:p.Gly610Ala | |
XM_017014551.1:c.1910G>C | XP_016870040.1:p.Gly637Ala | |
NM_001003800.2:c.1829G>C MANE Select | NP_001003800.1:p.Gly610Ala | |
NM_015250.4:c.1829G>C | NP_056065.1:p.Gly610Ala |