HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48304146C= , CM000675.2:g.48304146C= | GRCh38 |
NC_000013.10:g.48878282C= , CM000675.1:g.48878282C= | GRCh37 |
NC_000013.9:g.47776283C= | NCBI36 |
NG_009009.1:g.5400C= , LRG_517:g.5400C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.137+97C= MANE Select | ENSP00000267163.4:n.137+97C= | |
ENST00000646097.1:c.137+97C= | ENSP00000496556.1:n.137+97C= | |
ENST00000650461.1:c.137+97C= | ENSP00000497193.1:n.137+97C= | |
ENST00000267163.4:c.137+97C= | ENSP00000267163.4:n.137+97C= | |
ENST00000467505.5:c.137+97C= | ENSP00000434702.1:n.137+97C= | |
ENST00000525036.1:n.299+97C= | ||
NM_000321.2:c.137+97C= , LRG_517t1:c.137+97C= | NP_000312.2:n.137+97C= | |
NM_000321.3:c.137+97C= MANE Select | NP_000312.2:n.137+97C= |