HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94762910T>C , CM000672.2:g.94762910T>C | GRCh38 |
NC_000010.10:g.96522667T>C , CM000672.1:g.96522667T>C | GRCh37 |
NC_000010.9:g.96512657T>C | NCBI36 |
NG_008384.2:g.5205T>C | |
NG_008384.3:g.5230T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.168+37T>C MANE Select | ENSP00000360372.3:n.168+37T>C | |
ENST00000371321.7:c.168+37T>C | ENSP00000360372.3:n.168+37T>C | |
ENST00000464755.1:c.932-12148T>C | ENSP00000483243.1:n.932-12148T>C | |
ENST00000480405.2:c.168+37T>C | ENSP00000483847.1:n.168+37T>C | |
NM_000769.2:c.168+37T>C | NP_000760.1:n.168+37T>C | |
NM_000769.4:c.168+37T>C MANE Select | NP_000760.1:n.168+37T>C |