HGVS | Genome Assembly |
---|---|
NC_000001.11:g.56500640A>C , CM000663.2:g.56500640A>C | GRCh38 |
NC_000001.10:g.56966312A>C , CM000663.1:g.56966312A>C | GRCh37 |
NC_000001.9:g.56738900A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371250.4:c.811-3964T>G MANE Select | ENSP00000360296.3:n.811-3964T>G | |
ENST00000641109.1:c.220-3964T>G | ENSP00000493138.1:n.220-3964T>G | |
ENST00000641494.1:c.65-3964T>G | ||
ENST00000642129.1:c.455-3964T>G | ||
ENST00000371250.3:c.811-3964T>G | ENSP00000360296.3:n.811-3964T>G | |
ENST00000459962.1:n.1797-3964T>G | ||
ENST00000472957.1:n.296-3964T>G | ||
NM_003713.4:c.811-3964T>G | NP_003704.3:n.811-3964T>G | |
NM_003713.5:c.811-3964T>G MANE Select | NP_003704.3:n.811-3964T>G |