HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202377324T>C , CM000664.2:g.202377324T>C | GRCh38 |
NC_000002.11:g.203242047T>C , CM000664.1:g.203242047T>C | GRCh37 |
NC_000002.10:g.202950292T>C | NCBI36 |
NG_009363.1:g.5998T>C , LRG_712:g.5998T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.-151T>C MANE Select | ENSP00000363708.4:n.-151T>C | |
ENST00000374580.8:c.-151T>C | ENSP00000363708.4:n.-151T>C | |
NM_001204.6:c.-151T>C , LRG_712t1:c.-151T>C | NP_001195.2:n.-151T>C | |
XM_011511687.1:c.-151T>C | XP_011509989.1:n.-151T>C | |
XM_011511688.1:c.-151T>C | XP_011509990.1:n.-151T>C | |
NM_001204.7:c.-151T>C MANE Select | NP_001195.2:n.-151T>C |