HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177993138A>G , CM000667.2:g.177993138A>G | GRCh38 |
NC_000005.9:g.177420139A>G , CM000667.1:g.177420139A>G | GRCh37 |
NC_000005.8:g.177352745A>G | NCBI36 |
NG_015889.1:g.8105T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.343-91T>C MANE Select | ENSP00000311290.2:n.343-91T>C | |
NM_006261.4:c.343-91T>C | NP_006252.3:n.343-91T>C | |
NM_006261.5:c.343-91T>C MANE Select | NP_006252.4:n.343-91T>C |