HGVS | Genome Assembly |
---|---|
NC_000019.10:g.17824965T>C , CM000681.2:g.17824965T>C | GRCh38 |
NC_000019.9:g.17935774T>C , CM000681.1:g.17935774T>C | GRCh37 |
NC_000019.8:g.17796774T>C | NCBI36 |
NG_007273.1:g.28027A>G , LRG_77:g.28027A>G | |
NG_012092.1:g.1547A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696967.1:n.4330A>G | ||
ENST00000696968.1:n.2386A>G | ||
ENST00000458235.7:c.*1778A>G MANE Select | ENSP00000391676.1:n.*1778A>G | |
ENST00000458235.5:c.*1778A>G | ENSP00000391676.1:n.*1778A>G | |
ENST00000527031.5:n.2624A>G | ||
NM_000215.3:c.*1778A>G , LRG_77t1:c.*1778A>G | NP_000206.2:n.*1778A>G | |
XM_005259896.2:c.*1778A>G | XP_005259953.1:n.*1778A>G | |
XM_005259896.3:c.*1778A>G | XP_005259953.1:n.*1778A>G | |
NM_000215.4:c.*1778A>G MANE Select | NP_000206.2:n.*1778A>G |