HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115730842C>T , CM000663.2:g.115730842C>T | GRCh38 |
NC_000001.10:g.116273463C>T , CM000663.1:g.116273463C>T | GRCh37 |
NC_000001.9:g.116074986C>T | NCBI36 |
NG_008802.1:g.42964G>A , LRG_404:g.42964G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000488931.2:c.425+1272G>A | ENSP00000518226.1:n.425+1272G>A | |
ENST00000261448.6:c.606+2059G>A MANE Select | ENSP00000261448.5:n.606+2059G>A | |
ENST00000261448.5:c.606+2059G>A | ENSP00000261448.5:n.606+2059G>A | |
ENST00000488931.1:n.122+1272G>A | ||
NM_001232.3:c.606+2059G>A , LRG_404t1:c.606+2059G>A | NP_001223.2:n.606+2059G>A | |
NM_001232.4:c.606+2059G>A MANE Select | NP_001223.2:n.606+2059G>A |