HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189575148T= , CM000664.2:g.189575148T= | GRCh38 |
NC_000002.11:g.190439874T= , CM000664.1:g.190439874T= | GRCh37 |
NC_000002.10:g.190148119T= | NCBI36 |
NG_009027.1:g.10664A= , LRG_837:g.10664A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261024.7:c.271+13A= MANE Select | ENSP00000261024.3:n.271+13A= | |
ENST00000261024.6:c.271+13A= | ENSP00000261024.2:n.271+13A= | |
ENST00000427241.5:c.271+13A= | ENSP00000390005.1:n.271+13A= | |
ENST00000479598.5:n.552+13A= | ||
NM_014585.5:c.271+13A= , LRG_837t1:c.271+13A= | NP_055400.1:n.271+13A= | |
XM_005246505.1:c.151+13A= | XP_005246562.1:n.151+13A= | |
XM_005246505.2:c.151+13A= | XP_005246562.1:n.151+13A= | |
XM_017003938.2:c.151+13A= | XP_016859427.1:n.151+13A= | |
NM_014585.6:c.271+13A= MANE Select | NP_055400.1:n.271+13A= |