HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88007790C>G , CM000666.2:g.88007790C>G | GRCh38 |
NC_000004.11:g.88928942C>G , CM000666.1:g.88928942C>G | GRCh37 |
NC_000004.10:g.89147966C>G | NCBI36 |
NG_008604.1:g.5123C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.57C>G MANE Select | ENSP00000237596.2:p.Pro19= | |
ENST00000237596.6:c.57C>G | ENSP00000237596.2:p.Pro19= | |
NM_000297.3:c.57C>G | NP_000288.1:p.Pro19= | |
XM_011532028.1:c.57C>G | XP_011530330.1:p.Pro19= | |
XR_244632.2:n.152C>G | ||
NR_156488.1:n.144C>G | ||
XM_011532028.2:c.57C>G | XP_011530330.1:p.Pro19= | |
NM_000297.4:c.57C>G MANE Select | NP_000288.1:p.Pro19= | |
NR_156488.2:n.156C>G |