HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8076321G>A , CM000679.2:g.8076321G>A | GRCh38 |
NC_000017.10:g.7979639G>A , CM000679.1:g.7979639G>A | GRCh37 |
NC_000017.9:g.7920364G>A | NCBI36 |
NG_007099.1:g.16383C>T | |
NG_007099.2:g.16396C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647874.1:c.1386C>T MANE Select | ENSP00000497784.1:p.Gly462= | |
ENST00000649809.1:c.450C>T | ENSP00000496845.1:p.Gly150= | |
ENST00000319144.4:c.1386C>T | ENSP00000315167.4:p.Gly462= | |
ENST00000577351.5:n.333C>T | ||
ENST00000583276.5:n.770C>T | ||
ENST00000584116.1:n.642C>T | ||
NM_001139.2:c.1386C>T | NP_001130.1:p.Gly462= | |
NM_001139.3:c.1386C>T MANE Select | NP_001130.1:p.Gly462= |