HGVS | Genome Assembly |
---|---|
NC_000009.12:g.841831G>C , CM000671.2:g.841831G>C | GRCh38 |
NC_000009.11:g.841831G>C , CM000671.1:g.841831G>C | GRCh37 |
NC_000009.10:g.831831G>C | NCBI36 |
NG_009221.1:g.5142G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382276.8:c.-8G>C MANE Select | ENSP00000371711.3:n.-8G>C | |
ENST00000382276.7:c.-8G>C | ENSP00000371711.3:n.-8G>C | |
ENST00000564322.1:n.142G>C | ||
NM_021951.2:c.-8G>C | NP_068770.2:n.-8G>C | |
XM_006716732.1:c.-8G>C | XP_006716795.1:n.-8G>C | |
XM_017014375.1:c.-8G>C | XP_016869864.1:n.-8G>C | |
NM_021951.3:c.-8G>C MANE Select | NP_068770.2:n.-8G>C |