HGVS | Genome Assembly |
---|---|
NC_000007.14:g.141973348_141973365dup , CM000669.2:g.141973348_141973365dup | GRCh38 |
NC_000007.13:g.141673148_141673165dup , CM000669.1:g.141673148_141673165dup | GRCh37 |
NC_000007.12:g.141319617_141319634dup | NCBI36 |
NG_016141.1:g.5411_5428dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000465654.5:c.-3+27351_-3+27368dup (MGAM) | ENSP00000419372.1:n.-3+27351_-3+27368dup | |
ENST00000547270.1:c.327_344dup (TAS2R38) MANE Select | ENSP00000448219.1:p.Leu115_Leu116insAlaAl... | |
NM_176817.4:c.327_344dup (TAS2R38) | NP_789787.4:p.Leu115_Leu116insAlaAlaCysLe... | |
XM_011515783.1:c.*25-13048_*25-13031dup (OR9A4) | XP_011514085.1:n.*25-13048_*25-13031dup | |
NM_176817.5:c.327_344dup (TAS2R38) MANE Select | NP_789787.5:p.Leu115_Leu116insAlaAlaCysLe... |