HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94426252G= , CM000669.2:g.94426252G= | GRCh38 |
NC_000007.13:g.94055564G= , CM000669.1:g.94055564G= | GRCh37 |
NC_000007.12:g.93893500G= | NCBI36 |
NG_007405.1:g.36692G= , LRG_2:g.36692G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.2998-171G= MANE Select | ENSP00000297268.6:n.2998-171G= | |
ENST00000297268.10:c.2998-171G= | ENSP00000297268.6:n.2998-171G= | |
ENST00000478215.1:n.557-171G= | ||
ENST00000481570.5:n.2971-171G= | ||
ENST00000620463.1:c.2992-171G= | ENSP00000477719.1:n.2992-171G= | |
NM_000089.3:c.2998-171G= , LRG_2t1:c.2998-171G= | NP_000080.2:n.2998-171G= | |
NM_000089.4:c.2998-171G= MANE Select | NP_000080.2:n.2998-171G= |