HGVS | Genome Assembly |
---|---|
NC_000001.11:g.155225189T>C , CM000663.2:g.155225189T>C | GRCh38 |
NC_000001.9:g.153461604T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463838.6:n.158+2193A>G | ||
ENST00000688506.1:n.81+2193A>G | ||
ENST00000689837.1:n.132+2193A>G | ||
ENST00000691165.1:n.81+2193A>G | ||
ENST00000693149.1:n.81+2193A>G | ||
ENST00000693267.1:n.147+2193A>G | ||
ENST00000693749.1:n.132+2193A>G | ||
ENST00000368374.5:n.42-102A>G | ||
NR_002188.3:n.153+2193A>G |