HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584214T>A , CM000679.2:g.41584214T>A | GRCh38 |
NC_000017.10:g.39740466T>A , CM000679.1:g.39740466T>A | GRCh37 |
NC_000017.9:g.36993992T>A | NCBI36 |
NG_008624.1:g.7682A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.765+43A>T MANE Select | ENSP00000167586.6:n.765+43A>T | |
ENST00000167586.6:c.765+43A>T | ENSP00000167586.6:n.765+43A>T | |
ENST00000476662.1:n.215+43A>T | ||
NM_000526.4:c.765+43A>T | NP_000517.2:n.765+43A>T | |
NM_000526.5:c.765+43A>T MANE Select | NP_000517.3:n.765+43A>T |