HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320397A>G , CM000667.2:g.159320397A>G | GRCh38 |
NC_000005.9:g.158747405A>G , CM000667.1:g.158747405A>G | GRCh37 |
NC_000005.8:g.158679983A>G | NCBI36 |
NG_009618.1:g.15077T>C , LRG_71:g.15077T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.-25T>C | ENSP00000512849.1:n.-25T>C | |
ENST00000696751.1:c.*101T>C | ENSP00000512850.1:n.*101T>C | |
ENST00000231228.3:c.606T>C MANE Select | ENSP00000231228.2:p.Ala202= | |
ENST00000231228.2:c.606T>C | ENSP00000231228.2:p.Ala202= | |
NM_002187.2:c.606T>C , LRG_71t1:c.606T>C | NP_002178.2:p.Ala202= | |
NM_002187.3:c.606T>C MANE Select | NP_002178.2:p.Ala202= |