HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315925A>G , CM000667.2:g.159315925A>G | GRCh38 |
NC_000005.9:g.158742933A>G , CM000667.1:g.158742933A>G | GRCh37 |
NC_000005.8:g.158675511A>G | NCBI36 |
NG_009618.1:g.19549T>C , LRG_71:g.19549T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*176T>C | ENSP00000512849.1:n.*176T>C | |
ENST00000696751.1:c.*658T>C | ENSP00000512850.1:n.*658T>C | |
ENST00000231228.3:c.*176T>C MANE Select | ENSP00000231228.2:n.*176T>C | |
ENST00000231228.2:c.*176T>C | ENSP00000231228.2:n.*176T>C | |
NM_002187.2:c.*176T>C , LRG_71t1:c.*176T>C | NP_002178.2:n.*176T>C | |
NM_002187.3:c.*176T>C MANE Select | NP_002178.2:n.*176T>C |