HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48303801A>T , CM000675.2:g.48303801A>T | GRCh38 |
NC_000013.10:g.48877937A>T , CM000675.1:g.48877937A>T | GRCh37 |
NC_000013.9:g.47775938A>T | NCBI36 |
NG_009009.1:g.5055A>T , LRG_517:g.5055A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.-112A>T MANE Select | ENSP00000267163.4:n.-112A>T | |
ENST00000646097.1:c.-112A>T | ENSP00000496556.1:n.-112A>T | |
ENST00000650461.1:c.-112A>T | ENSP00000497193.1:n.-112A>T | |
ENST00000267163.4:c.-112A>T | ENSP00000267163.4:n.-112A>T | |
ENST00000467505.5:c.-112A>T | ENSP00000434702.1:n.-112A>T | |
ENST00000525036.1:n.51A>T | ||
NM_000321.2:c.-112A>T , LRG_517t1:c.-112A>T | NP_000312.2:n.-112A>T | |
NM_000321.3:c.-112A>T MANE Select | NP_000312.2:n.-112A>T |