HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240877357T>A , CM000664.2:g.240877357T>A | GRCh38 |
NC_000002.11:g.241816774T>A , CM000664.1:g.241816774T>A | GRCh37 |
NC_000002.10:g.241465447T>A | NCBI36 |
NG_008005.1:g.13613T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.847-180T>A MANE Select | ENSP00000302620.3:n.847-180T>A | |
ENST00000307503.3:c.847-180T>A | ENSP00000302620.3:n.847-180T>A | |
ENST00000470255.1:n.445T>A | ||
NM_000030.2:c.847-180T>A | NP_000021.1:n.847-180T>A | |
NM_000030.3:c.847-180T>A MANE Select | NP_000021.1:n.847-180T>A |