HGVS | Genome Assembly |
---|---|
NC_000014.9:g.77518113A>G , CM000676.2:g.77518113A>G | GRCh38 |
NC_000014.8:g.77984456A>G , CM000676.1:g.77984456A>G | GRCh37 |
NC_000014.7:g.77054209A>G | NCBI36 |
NG_028282.1:g.103655T>C , LRG_371:g.103655T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686627.1:n.526T>C | ||
ENST00000687688.1:n.1257T>C | ||
ENST00000692906.1:n.1226T>C | ||
ENST00000216484.7:c.1494T>C MANE Select | ENSP00000216484.2:p.Phe498= | |
ENST00000216484.6:c.1494T>C | ENSP00000216484.2:p.Phe498= | |
ENST00000556607.1:c.322T>C | ENSP00000451029.1:n.322T>C | |
NM_004863.3:c.1494T>C , LRG_371t1:c.1494T>C | NP_004854.1:p.Phe498= | |
NM_004863.4:c.1494T>C MANE Select | NP_004854.1:p.Phe498= |