HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75003555C>T , CM000676.2:g.75003555C>T | GRCh38 |
NC_000014.8:g.75470258C>T , CM000676.1:g.75470258C>T | GRCh37 |
NC_000014.7:g.74540011C>T | NCBI36 |
NG_013333.1:g.5647C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.289C>T MANE Select | ENSP00000266126.5:p.His97Tyr | |
ENST00000266126.9:c.289C>T | ENSP00000266126.5:p.His97Tyr | |
ENST00000553401.5:c.262C>T | ENSP00000451681.1:p.His88Tyr | |
ENST00000553539.1:n.584C>T | ||
ENST00000555522.1:n.347C>T | ||
ENST00000556028.5:c.289C>T | ENSP00000452311.1:p.His97Tyr | |
NM_014239.3:c.289C>T | NP_055054.1:p.His97Tyr | |
NM_014239.4:c.289C>T MANE Select | NP_055054.1:p.His97Tyr |