HGVS | Genome Assembly |
---|---|
NC_000017.11:g.73196646A>C , CM000679.2:g.73196646A>C | GRCh38 |
NC_000017.10:g.71192785A>C , CM000679.1:g.71192785A>C | GRCh37 |
NC_000017.9:g.68704380A>C | NCBI36 |
NG_008971.1:g.8613A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000299886.9:c.455A>C MANE Select | ENSP00000299886.4:p.His152Pro | |
ENST00000299886.8:c.455A>C | ENSP00000299886.4:p.His152Pro | |
ENST00000438720.7:c.453A>C | ||
ENST00000582587.2:c.452A>C | ||
ENST00000618996.4:c.455A>C | ENSP00000479450.1:p.His152Pro | |
NM_018714.2:c.455A>C | NP_061184.1:p.His152Pro | |
NM_018714.3:c.455A>C MANE Select | NP_061184.1:p.His152Pro |