HGVS | Genome Assembly |
---|---|
NC_000016.10:g.23416916A>C , CM000678.2:g.23416916A>C | GRCh38 |
NC_000016.9:g.23428237A>C , CM000678.1:g.23428237A>C | GRCh37 |
NC_000016.8:g.23335738A>C | NCBI36 |
NG_021287.1:g.41276T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307149.10:c.1292+51T>G MANE Select | ENSP00000305442.5:n.1292+51T>G | |
ENST00000307149.9:c.1292+51T>G | ENSP00000305442.5:n.1292+51T>G | |
ENST00000567821.1:n.327+51T>G | ||
NM_153603.3:c.1292+51T>G | NP_705831.1:n.1292+51T>G | |
XR_429680.1:n.1508+51T>G | ||
XM_017023870.1:c.1097+51T>G | XP_016879359.1:n.1097+51T>G | |
XR_002957852.1:n.1513+51T>G | ||
XR_429680.2:n.1513+51T>G | ||
NM_153603.4:c.1292+51T>G MANE Select | NP_705831.1:n.1292+51T>G |