HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240875050T>C , CM000664.2:g.240875050T>C | GRCh38 |
NC_000002.11:g.241814467T>C , CM000664.1:g.241814467T>C | GRCh37 |
NC_000002.10:g.241463140T>C | NCBI36 |
NG_008005.1:g.11306T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.681-59T>C MANE Select | ENSP00000302620.3:n.681-59T>C | |
ENST00000307503.3:c.681-59T>C | ENSP00000302620.3:n.681-59T>C | |
ENST00000476698.1:n.333-59T>C | ||
NM_000030.2:c.681-59T>C | NP_000021.1:n.681-59T>C | |
NM_000030.3:c.681-59T>C MANE Select | NP_000021.1:n.681-59T>C |