HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992925A>G , CM000667.2:g.177992925A>G | GRCh38 |
NC_000005.9:g.177419926A>G , CM000667.1:g.177419926A>G | GRCh37 |
NC_000005.8:g.177352532A>G | NCBI36 |
NG_015889.1:g.8318T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.465T>C MANE Select | ENSP00000311290.2:p.Tyr155= | |
NM_006261.4:c.465T>C | NP_006252.3:p.Tyr155= | |
NM_006261.5:c.465T>C MANE Select | NP_006252.4:p.Tyr155= |