HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55368505G>C , CM000681.2:g.55368505G>C | GRCh38 |
NC_000019.9:g.55879873G>C , CM000681.1:g.55879873G>C | GRCh37 |
NC_000019.8:g.60571685G>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264563.7:c.245C>G MANE Select | ENSP00000264563.1:p.Ala82Gly | |
ENST00000264563.6:c.245C>G | ENSP00000264563.1:p.Ala82Gly | |
ENST00000585513.1:c.245C>G | ENSP00000467355.1:p.Ala82Gly | |
ENST00000587093.1:c.8C>G | ENSP00000468663.1:p.Ala3Gly | |
ENST00000590625.5:c.8C>G | ENSP00000465705.1:p.Ala3Gly | |
NM_000641.3:c.245C>G | NP_000632.1:p.Ala82Gly | |
NM_001267718.1:c.8C>G | NP_001254647.1:p.Ala3Gly | |
NM_000641.4:c.245C>G MANE Select | NP_000632.1:p.Ala82Gly | |
NM_001267718.2:c.8C>G | NP_001254647.1:p.Ala3Gly |