HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157109222A>C , CM000667.2:g.157109222A>C | GRCh38 |
NC_000005.9:g.156536233A>C , CM000667.1:g.156536233A>C | GRCh37 |
NC_000005.8:g.156468811A>C | NCBI36 |
NG_030444.1:g.5016T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524219.2:c.-293-2260T>G | ENSP00000430328.2:n.-293-2260T>G | |
ENST00000696899.1:c.-239T>G | ENSP00000512960.1:n.-239T>G | |
ENST00000696900.1:c.-834T>G | ENSP00000512961.1:n.-834T>G | |
ENST00000696901.1:c.-239T>G | ENSP00000512962.1:n.-239T>G | |
ENST00000307851.8:c.-239T>G | ENSP00000312002.4:n.-239T>G | |
ENST00000524219.1:c.-293-2260T>G | ENSP00000430328.1:n.-293-2260T>G | |
NM_032782.4:c.-239T>G | NP_116171.3:n.-239T>G |