HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141972722_141972725dup , CM000669.2:g.141972722_141972725dup | GRCh38 |
NC_000007.13:g.141672522_141672525dup , CM000669.1:g.141672522_141672525dup | GRCh37 |
NC_000007.12:g.141318991_141318994dup | NCBI36 |
NG_016141.1:g.6049_6052dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000465654.5:c.-3+26725_-3+26728dup (MGAM) | ENSP00000419372.1:n.-3+26725_-3+26728dup | |
ENST00000547270.1:c.965_968dup (TAS2R38) MANE Select | ENSP00000448219.1:p.Asp324SerfsTer18 | |
NM_176817.4:c.965_968dup (TAS2R38) | NP_789787.4:p.Asp324SerfsTer18 | |
XM_011515783.1:c.*25-13674_*25-13671dup (OR9A4) | XP_011514085.1:n.*25-13674_*25-13671dup | |
NM_176817.5:c.965_968dup (TAS2R38) MANE Select | NP_789787.5:p.Asp324SerfsTer18 |