HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7529841A>T , CM000681.2:g.7529841A>T | GRCh38 |
NC_000019.9:g.7594727A>T , CM000681.1:g.7594727A>T | GRCh37 |
NC_000019.8:g.7500727A>T | NCBI36 |
NG_013374.1:g.690A>T | |
NG_015806.1:g.12232A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.1359+129A>T MANE Select | ENSP00000264079.5:n.1359+129A>T | |
ENST00000264079.10:c.1359+129A>T | ENSP00000264079.5:n.1359+129A>T | |
ENST00000394321.9:n.1674+129A>T | ||
ENST00000594692.1:n.355+129A>T | ||
ENST00000595860.5:n.542+129A>T | ||
ENST00000599334.1:c.236+129A>T | ||
NM_020533.2:c.1359+129A>T | NP_065394.1:n.1359+129A>T | |
NM_020533.3:c.1359+129A>T MANE Select | NP_065394.1:n.1359+129A>T |