HGVS | Genome Assembly |
---|---|
NC_000016.10:g.172968G>C , CM000678.2:g.172968G>C | GRCh38 |
NC_000016.9:g.222967G>C , CM000678.1:g.222967G>C | GRCh37 |
NC_000016.8:g.162967G>C | NCBI36 |
NG_000006.1:g.33831G>C | |
NG_059186.1:g.1318G>C | |
NG_059271.1:g.5122G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251595.11:c.56G>C MANE Select | ENSP00000251595.6:p.Gly19Ala | |
ENST00000251595.10:c.56G>C | ENSP00000251595.6:p.Gly19Ala | |
ENST00000397806.1:c.-2+10G>C | ENSP00000380908.1:n.-2+10G>C | |
ENST00000482565.1:n.75G>C | ||
ENST00000484216.1:n.25G>C | ||
NM_000517.4:c.56G>C | NP_000508.1:p.Gly19Ala | |
NM_000517.6:c.56G>C MANE Select | NP_000508.1:p.Gly19Ala |