HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75003558G>T , CM000676.2:g.75003558G>T | GRCh38 |
NC_000014.8:g.75470261G>T , CM000676.1:g.75470261G>T | GRCh37 |
NC_000014.7:g.74540014G>T | NCBI36 |
NG_013333.1:g.5650G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.292G>T MANE Select | ENSP00000266126.5:p.Gly98Ter | |
ENST00000266126.9:c.292G>T | ENSP00000266126.5:p.Gly98Ter | |
ENST00000553401.5:c.265G>T | ENSP00000451681.1:p.Gly89Ter | |
ENST00000553539.1:n.587G>T | ||
ENST00000555522.1:n.350G>T | ||
ENST00000556028.5:c.292G>T | ENSP00000452311.1:p.Gly98Ter | |
NM_014239.3:c.292G>T | NP_055054.1:p.Gly98Ter | |
NM_014239.4:c.292G>T MANE Select | NP_055054.1:p.Gly98Ter |