HGVS | Genome Assembly |
---|---|
NC_000023.11:g.68829864A>C , CM000685.2:g.68829864A>C | GRCh38 |
NC_000023.10:g.68049707A>C , CM000685.1:g.68049707A>C | GRCh37 |
NC_000023.9:g.67966432A>C | NCBI36 |
NG_008887.1:g.5868A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000204961.5:c.88A>C MANE Select | ENSP00000204961.4:p.Lys30Gln | |
ENST00000204961.4:c.88A>C | ENSP00000204961.4:p.Lys30Gln | |
NM_004429.4:c.88A>C | NP_004420.1:p.Lys30Gln | |
NM_004429.5:c.88A>C MANE Select | NP_004420.1:p.Lys30Gln |