HGVS | Genome Assembly |
---|---|
NC_000019.10:g.41348319C>A , CM000681.2:g.41348319C>A | GRCh38 |
NC_000019.9:g.41854224C>A , CM000681.1:g.41854224C>A | GRCh37 |
NC_000019.8:g.46546064C>A | NCBI36 |
NG_013364.1:g.10608G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221930.6:c.492G>T MANE Select | ENSP00000221930.4:p.Val164= | |
ENST00000600196.2:c.492G>T | ENSP00000504008.1:p.Val164= | |
ENST00000677934.1:c.492G>T | ENSP00000504769.1:p.Val164= | |
ENST00000221930.5:c.492G>T | ENSP00000221930.4:p.Val164= | |
ENST00000597453.1:n.23G>T | ||
NM_000660.5:c.492G>T | NP_000651.3:p.Val164= | |
XM_011527242.1:c.492G>T | XP_011525544.1:p.Val164= | |
NM_000660.6:c.492G>T | NP_000651.3:p.Val164= | |
XM_011527242.2:c.492G>T | XP_011525544.1:p.Val164= | |
NM_000660.7:c.492G>T MANE Select | NP_000651.3:p.Val164= |