HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67583831A>C , CM000673.2:g.67583831A>C | GRCh38 |
NC_000011.9:g.67351302A>C , CM000673.1:g.67351302A>C | GRCh37 |
NC_000011.8:g.67107878A>C | NCBI36 |
NG_012075.1:g.5237A>C , LRG_723:g.5237A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.-13A>C | ENSP00000381604.1:n.-13A>C | |
ENST00000398606.10:c.-13A>C MANE Select | ENSP00000381607.3:n.-13A>C | |
ENST00000646888.1:c.-13A>C | ENSP00000494477.1:n.-13A>C | |
ENST00000398603.5:c.-13A>C | ENSP00000381604.1:n.-13A>C | |
ENST00000398606.7:c.-13A>C | ENSP00000381607.3:n.-13A>C | |
ENST00000494593.1:n.10A>C | ||
NM_000852.3:c.-13A>C , LRG_723t1:c.-13A>C | NP_000843.1:n.-13A>C | |
NM_000852.4:c.-13A>C MANE Select | NP_000843.1:n.-13A>C |