HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40844998G>A , CM000681.2:g.40844998G>A | GRCh38 |
NC_000019.9:g.41350903G>A , CM000681.1:g.41350903G>A | GRCh37 |
NC_000019.8:g.46042743G>A | NCBI36 |
NG_008377.1:g.10450C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301141.10:c.1162-226C>T MANE Select | ENSP00000301141.4:n.1162-226C>T | |
ENST00000301141.9:c.1162-226C>T | ENSP00000301141.4:n.1162-226C>T | |
ENST00000596719.5:n.1308C>T | ||
ENST00000601627.1:c.119+43583G>A | ||
ENST00000610301.1:c.1162-226C>T | ENSP00000477899.1:n.1162-226C>T | |
NM_000762.5:c.1162-226C>T | NP_000753.3:n.1162-226C>T | |
NM_000762.6:c.1162-226C>T MANE Select | NP_000753.3:n.1162-226C>T |