HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400566A>C , CM000670.2:g.18400566A>C | GRCh38 |
NC_000008.10:g.18258076A>C , CM000670.1:g.18258076A>C | GRCh37 |
NC_000008.9:g.18302356A>C | NCBI36 |
NG_012246.1:g.14322A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286479.4:c.563A>C MANE Select | ENSP00000286479.3:p.Lys188Thr | |
ENST00000286479.3:c.563A>C | ENSP00000286479.3:p.Lys188Thr | |
ENST00000520116.1:c.173A>C | ENSP00000428416.1:p.Lys58Thr | |
NM_000015.2:c.563A>C | NP_000006.2:p.Lys188Thr | |
XM_011544358.1:c.563A>C | XP_011542660.1:p.Lys188Thr | |
XM_017012938.1:c.563A>C | XP_016868427.1:p.Lys188Thr | |
NM_000015.3:c.563A>C MANE Select | NP_000006.2:p.Lys188Thr |