HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161363401A= , CM000663.2:g.161363401A= | GRCh38 |
NC_000001.10:g.161333191A= , CM000663.1:g.161333191A= | GRCh37 |
NC_000001.9:g.159599815A= | NCBI36 |
NG_012767.1:g.54026A= , LRG_317:g.54026A= |
HGVS | Amino-acid Change |
---|---|
NM_001035511.1:c.*861A= | NP_001030588.1:n.*861A= |
NM_001035511.2:c.*861A= | NP_001030588.1:n.*861A= |
NM_001035512.1:c.*968A= | NP_001030589.1:n.*968A= |
NM_001035512.2:c.*968A= | NP_001030589.1:n.*968A= |
NM_001035513.1:c.*968A= | NP_001030590.1:n.*968A= |
NM_001035513.2:c.*968A= | NP_001030590.1:n.*968A= |
NM_001278172.1:c.*861A= | NP_001265101.1:n.*861A= |
NM_001278172.2:c.*861A= | NP_001265101.1:n.*861A= |
NM_003001.3:c.*968A= , LRG_317t1:c.*968A= | NP_002992.1:n.*968A= |
NR_103459.1:n.1535A= | |
NR_103459.2:n.1530A= | |
ENST00000367975.6:c.*968A= | ENSP00000356953.2:n.*968A= |