HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008041T>G , CM000666.2:g.88008041T>G | GRCh38 |
NC_000004.11:g.88929193T>G , CM000666.1:g.88929193T>G | GRCh37 |
NC_000004.10:g.89148217T>G | NCBI36 |
NG_008604.1:g.5374T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.308T>G MANE Select | ENSP00000237596.2:p.Val103Gly | |
ENST00000237596.6:c.308T>G | ENSP00000237596.2:p.Val103Gly | |
NM_000297.3:c.308T>G | NP_000288.1:p.Val103Gly | |
XM_011532028.1:c.308T>G | XP_011530330.1:p.Val103Gly | |
XR_244632.2:n.403T>G | ||
NR_156488.1:n.395T>G | ||
XM_011532028.2:c.308T>G | XP_011530330.1:p.Val103Gly | |
NM_000297.4:c.308T>G MANE Select | NP_000288.1:p.Val103Gly | |
NR_156488.2:n.407T>G |