HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927726C>G , CM000663.2:g.149927726C>G | GRCh38 |
NC_000001.10:g.149899618C>G , CM000663.1:g.149899618C>G | GRCh37 |
NC_000001.9:g.148166242C>G | NCBI36 |
NG_032777.1:g.5527G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.34G>C MANE Select | ENSP00000271628.8:p.Asp12His | |
ENST00000271628.8:c.34G>C | ENSP00000271628.8:p.Asp12His | |
NM_005850.4:c.34G>C | NP_005841.1:p.Asp12His | |
NM_005850.5:c.34G>C MANE Select | NP_005841.1:p.Asp12His |