HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1394935C>A , CM000667.2:g.1394935C>A | GRCh38 |
NC_000005.9:g.1395050C>A , CM000667.1:g.1395050C>A | GRCh37 |
NC_000005.8:g.1448050C>A | NCBI36 |
NG_015885.1:g.55494G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.1840-177G>T MANE Select | ENSP00000270349.9:n.1840-177G>T | |
ENST00000270349.11:c.1840-177G>T | ENSP00000270349.9:n.1840-177G>T | |
ENST00000512002.2:n.221-177G>T | ||
NM_001044.4:c.1840-177G>T | NP_001035.1:n.1840-177G>T | |
NM_001044.5:c.1840-177G>T MANE Select | NP_001035.1:n.1840-177G>T |