HGVS | Genome Assembly |
---|---|
NC_000019.10:g.17811986G>C , CM000681.2:g.17811986G>C | GRCh38 |
NC_000019.9:g.17922795G>C , CM000681.1:g.17922795G>C | GRCh37 |
NC_000019.8:g.17783795G>C | NCBI36 |
NG_028981.1:g.21877G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000318683.7:c.983G>C MANE Select | ENSP00000321874.5:p.Arg328Pro | |
ENST00000318683.6:c.983G>C | ENSP00000321874.5:p.Arg328Pro | |
ENST00000595387.1:c.983G>C | ENSP00000472638.1:p.Arg328Pro | |
NM_014256.3:c.983G>C | NP_055071.2:p.Arg328Pro | |
XM_011527626.1:c.983G>C | XP_011525928.1:p.Arg328Pro | |
XM_011527627.1:c.983G>C | XP_011525929.1:p.Arg328Pro | |
XM_011527626.2:c.983G>C | XP_011525928.1:p.Arg328Pro | |
NM_014256.4:c.983G>C MANE Select | NP_055071.2:p.Arg328Pro |