HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115731247A>G , CM000663.2:g.115731247A>G | GRCh38 |
NC_000001.10:g.116273868A>G , CM000663.1:g.116273868A>G | GRCh37 |
NC_000001.9:g.116075391A>G | NCBI36 |
NG_008802.1:g.42559T>C , LRG_404:g.42559T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000488931.2:c.425+867T>C | ENSP00000518226.1:n.425+867T>C | |
ENST00000261448.6:c.606+1654T>C MANE Select | ENSP00000261448.5:n.606+1654T>C | |
ENST00000261448.5:c.606+1654T>C | ENSP00000261448.5:n.606+1654T>C | |
ENST00000488931.1:n.122+867T>C | ||
NM_001232.3:c.606+1654T>C , LRG_404t1:c.606+1654T>C | NP_001223.2:n.606+1654T>C | |
NM_001232.4:c.606+1654T>C MANE Select | NP_001223.2:n.606+1654T>C |