HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400739T>C , CM000670.2:g.18400739T>C | GRCh38 |
NC_000008.10:g.18258249T>C , CM000670.1:g.18258249T>C | GRCh37 |
NC_000008.9:g.18302529T>C | NCBI36 |
NG_012246.1:g.14495T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286479.4:c.736T>C MANE Select | ENSP00000286479.3:p.Tyr246His | |
ENST00000286479.3:c.736T>C | ENSP00000286479.3:p.Tyr246His | |
ENST00000520116.1:c.346T>C | ENSP00000428416.1:p.Tyr116His | |
NM_000015.2:c.736T>C | NP_000006.2:p.Tyr246His | |
XM_011544358.1:c.736T>C | XP_011542660.1:p.Tyr246His | |
XM_017012938.1:c.736T>C | XP_016868427.1:p.Tyr246His | |
NM_000015.3:c.736T>C MANE Select | NP_000006.2:p.Tyr246His |