HGVS | Genome Assembly |
---|---|
NC_000016.10:g.23416925G= , CM000678.2:g.23416925G= | GRCh38 |
NC_000016.9:g.23428246G= , CM000678.1:g.23428246G= | GRCh37 |
NC_000016.8:g.23335747G= | NCBI36 |
NG_021287.1:g.41267C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307149.10:c.1292+42C= MANE Select | ENSP00000305442.5:n.1292+42C= | |
ENST00000307149.9:c.1292+42C= | ENSP00000305442.5:n.1292+42C= | |
ENST00000567821.1:n.327+42C= | ||
NM_153603.3:c.1292+42C= | NP_705831.1:n.1292+42C= | |
XR_429680.1:n.1508+42C= | ||
XM_017023870.1:c.1097+42C= | XP_016879359.1:n.1097+42C= | |
XR_002957852.1:n.1513+42C= | ||
XR_429680.2:n.1513+42C= | ||
NM_153603.4:c.1292+42C= MANE Select | NP_705831.1:n.1292+42C= |