HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38071191G>C , CM000664.2:g.38071191G>C | GRCh38 |
NC_000002.11:g.38298334G>C , CM000664.1:g.38298334G>C | GRCh37 |
NC_000002.10:g.38151838G>C | NCBI36 |
NG_008386.2:g.9911C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490576.2:c.1163C>G | ENSP00000478839.2:p.Ala388Gly | |
ENST00000610745.5:c.1163C>G MANE Select | ENSP00000478561.1:p.Ala388Gly | |
ENST00000492443.1:n.541C>G | ||
ENST00000494864.1:c.50C>G | ENSP00000479876.1:p.Ala17Gly | |
ENST00000610745.4:c.1163C>G | ENSP00000478561.1:p.Ala388Gly | |
ENST00000613082.1:n.558C>G | ||
ENST00000614273.1:c.1163C>G | ENSP00000483678.1:p.Ala388Gly | |
NM_000104.3:c.1163C>G | NP_000095.2:p.Ala388Gly | |
NM_000104.4:c.1163C>G MANE Select | NP_000095.2:p.Ala388Gly |