HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48410548A>G , CM000677.2:g.48410548A>G | GRCh38 |
NC_000015.9:g.48702745A>G , CM000677.1:g.48702745A>G | GRCh37 |
NC_000015.8:g.46490037A>G | NCBI36 |
NG_008805.2:g.240241T>C , LRG_778:g.240241T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1866T>C | ENSP00000453958.2:n.*1866T>C | |
ENST00000682158.1:n.2439T>C | ||
ENST00000682170.1:n.3239T>C | ||
ENST00000682767.1:n.2355T>C | ||
ENST00000316623.10:c.*442T>C MANE Select | ENSP00000325527.5:n.*442T>C | |
ENST00000316623.9:c.*442T>C | ENSP00000325527.5:n.*442T>C | |
ENST00000559133.5:c.4427T>C | ||
NM_000138.4:c.*442T>C , LRG_778t1:c.*442T>C | NP_000129.3:n.*442T>C | |
NM_000138.5:c.*442T>C MANE Select | NP_000129.3:n.*442T>C |