HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240873194T>C , CM000664.2:g.240873194T>C | GRCh38 |
NC_000002.11:g.241812611T>C , CM000664.1:g.241812611T>C | GRCh37 |
NC_000002.10:g.241461284T>C | NCBI36 |
NG_008005.1:g.9450T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.595+145T>C MANE Select | ENSP00000302620.3:n.595+145T>C | |
ENST00000307503.3:c.595+145T>C | ENSP00000302620.3:n.595+145T>C | |
ENST00000472436.1:n.760T>C | ||
ENST00000476698.1:n.332+145T>C | ||
NM_000030.2:c.595+145T>C | NP_000021.1:n.595+145T>C | |
NM_000030.3:c.595+145T>C MANE Select | NP_000021.1:n.595+145T>C |