HGVS | Genome Assembly |
---|---|
NC_000006.12:g.38703061G>A , CM000668.2:g.38703061G>A | GRCh38 |
NC_000006.11:g.38670837G>A , CM000668.1:g.38670837G>A | GRCh37 |
NC_000006.10:g.38778815G>A | NCBI36 |
NG_012074.1:g.5116C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373365.5:c.-7C>T MANE Select | ENSP00000362463.3:n.-7C>T | |
ENST00000373365.4:c.-7C>T | ENSP00000362463.3:n.-7C>T | |
NM_006708.2:c.-7C>T | NP_006699.2:n.-7C>T | |
NM_006708.3:c.-7C>T MANE Select | NP_006699.2:n.-7C>T |