HGVS | Genome Assembly |
---|---|
NC_000001.11:g.206775974T= , CM000663.2:g.206775974T= | GRCh38 |
NC_000001.10:g.206949319T= , CM000663.1:g.206949319T= | GRCh37 |
NC_000001.9:g.205015942T= | NCBI36 |
NG_012088.1:g.1521A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000659997.3:c.-149+4896T= MANE Select | ENSP00000499459.2:n.-149+4896T= | |
ENST00000656872.2:c.-149+5144T= | ENSP00000499487.2:n.-149+5144T= | |
ENST00000659997.2:c.-149+4896T= | ENSP00000499459.2:n.-149+4896T= | |
ENST00000662320.1:n.67+5144T= | ||
NM_153758.3:c.-35+4896T= | NP_715639.1:n.-35+4896T= | |
NM_001393490.1:c.-149+5144T= | NP_001380419.1:n.-149+5144T= | |
NM_153758.5:c.-149+4896T= MANE Select | NP_715639.2:n.-149+4896T= |