HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116830652G>C , CM000673.2:g.116830652G>C | GRCh38 |
NC_000011.9:g.116701368G>C , CM000673.1:g.116701368G>C | GRCh37 |
NC_000011.8:g.116206578G>C | NCBI36 |
NG_008949.1:g.5745G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000227667.8:c.55+15G>C MANE Select | ENSP00000227667.2:n.55+15G>C | |
ENST00000227667.7:c.55+15G>C | ENSP00000227667.2:n.55+15G>C | |
ENST00000375345.3:c.109+15G>C | ENSP00000364494.1:n.109+15G>C | |
ENST00000433777.5:c.55+15G>C | ENSP00000410614.1:n.55+15G>C | |
ENST00000470144.1:n.87+15G>C | ||
ENST00000630701.1:c.109+15G>C | ENSP00000486182.1:n.109+15G>C | |
NM_000040.1:c.55+15G>C | NP_000031.1:n.55+15G>C | |
NM_000040.2:c.55+15G>C | NP_000031.1:n.55+15G>C | |
NM_000040.3:c.55+15G>C MANE Select | NP_000031.1:n.55+15G>C |