HGVS | Genome Assembly |
---|---|
NC_000023.11:g.44540995A>G , CM000685.2:g.44540995A>G | GRCh38 |
NC_000023.10:g.44400241A>G , CM000685.1:g.44400241A>G | GRCh37 |
NC_000023.9:g.44285185A>G | NCBI36 |
NG_021288.1:g.6981T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378045.5:c.185+950T>C MANE Select | ENSP00000367284.4:n.185+950T>C | |
ENST00000378045.4:c.185+950T>C | ENSP00000367284.4:n.185+950T>C | |
ENST00000483115.1:n.360+950T>C | ||
NM_173794.3:c.185+950T>C | NP_776155.1:n.185+950T>C | |
NM_173794.4:c.185+950T>C MANE Select | NP_776155.1:n.185+950T>C |