HGVS | Genome Assembly |
---|---|
NC_000001.11:g.10972882T>G , CM000663.2:g.10972882T>G | GRCh38 |
NC_000001.10:g.11032939T>G , CM000663.1:g.11032939T>G | GRCh37 |
NC_000001.9:g.10955526T>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000377004.9:c.128-2793A>C MANE Select | ENSP00000366203.4:n.128-2793A>C | |
ENST00000377004.8:c.128-2793A>C | ENSP00000366203.4:n.128-2793A>C | |
ENST00000520253.1:c.61-2793A>C | ||
NM_001170754.1:c.128-2793A>C | NP_001164225.1:n.128-2793A>C | |
NM_001170754.2:c.128-2793A>C MANE Select | NP_001164225.1:n.128-2793A>C |