HGVS | Genome Assembly |
---|---|
NC_000010.11:g.16836338C>G , CM000672.2:g.16836338C>G | GRCh38 |
NC_000010.10:g.16878337C>G , CM000672.1:g.16878337C>G | GRCh37 |
NC_000010.9:g.16918343C>G | NCBI36 |
NG_008967.1:g.298480G>C , LRG_540:g.298480G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377833.10:c.10077G>C MANE Select | ENSP00000367064.4:p.Ser3359= | |
ENST00000377833.8:c.10077G>C | ENSP00000367064.4:p.Ser3359= | |
NM_001081.3:c.10077G>C , LRG_540t1:c.10077G>C | NP_001072.2:p.Ser3359= | |
XM_011519709.1:c.6063G>C | XP_011518011.1:p.Ser2021= | |
XM_011519710.1:c.6039G>C | XP_011518012.1:p.Ser2013= | |
XM_011519711.1:c.5919G>C | XP_011518013.1:p.Ser1973= | |
XM_011519709.2:c.6063G>C | XP_011518011.1:p.Ser2021= | |
XM_011519710.2:c.6039G>C | XP_011518012.1:p.Ser2013= | |
XM_011519711.3:c.5919G>C | XP_011518013.1:p.Ser1973= | |
NM_001081.4:c.10077G>C MANE Select | NP_001072.2:p.Ser3359= |