HGVS | Genome Assembly |
---|---|
NC_000009.12:g.841881G>C , CM000671.2:g.841881G>C | GRCh38 |
NC_000009.11:g.841881G>C , CM000671.1:g.841881G>C | GRCh37 |
NC_000009.10:g.831881G>C | NCBI36 |
NG_009221.1:g.5192G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382276.8:c.43G>C MANE Select | ENSP00000371711.3:p.Glu15Gln | |
ENST00000382276.7:c.43G>C | ENSP00000371711.3:p.Glu15Gln | |
ENST00000564322.1:n.192G>C | ||
NM_021951.2:c.43G>C | NP_068770.2:p.Glu15Gln | |
XM_006716732.1:c.43G>C | XP_006716795.1:p.Glu15Gln | |
XM_017014375.1:c.43G>C | XP_016869864.1:p.Glu15Gln | |
NM_021951.3:c.43G>C MANE Select | NP_068770.2:p.Glu15Gln |