HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1411091A>G , CM000667.2:g.1411091A>G | GRCh38 |
NC_000005.9:g.1411206A>G , CM000667.1:g.1411206A>G | GRCh37 |
NC_000005.8:g.1464206A>G | NCBI36 |
NG_015885.1:g.39338T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.1269+152T>C MANE Select | ENSP00000270349.9:n.1269+152T>C | |
ENST00000270349.11:c.1269+152T>C | ENSP00000270349.9:n.1269+152T>C | |
NM_001044.4:c.1269+152T>C | NP_001035.1:n.1269+152T>C | |
NM_001044.5:c.1269+152T>C MANE Select | NP_001035.1:n.1269+152T>C |