HGVS | Genome Assembly |
---|---|
NC_000001.11:g.145790152T>C , CM000663.2:g.145790152T>C | GRCh38 |
NC_000001.10:g.145644929A>G , CM000663.1:g.145644929A>G | GRCh37 |
NC_000001.9:g.144356286A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000582693.5:c.103-1186A>G MANE Select | ENSP00000463650.1:n.103-1186A>G | |
ENST00000582693.4:c.103-1186A>G | ENSP00000463650.1:n.103-1186A>G | |
NM_014455.3:c.103-1186A>G | NP_055270.1:n.103-1186A>G | |
XM_005272952.3:c.-49-1186A>G | XP_005273009.1:n.-49-1186A>G | |
XM_011509419.1:c.103-1186A>G | XP_011507721.1:n.103-1186A>G | |
XM_005272952.5:c.-49-1186A>G | XP_005273009.1:n.-49-1186A>G | |
XR_001737118.2:n.302-1186A>G | ||
NM_014455.4:c.103-1186A>G MANE Select | NP_055270.1:n.103-1186A>G |