HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47733466G>C , CM000679.2:g.47733466G>C | GRCh38 |
NC_000017.10:g.45810832G>C , CM000679.1:g.45810832G>C | GRCh37 |
NC_000017.9:g.43165831G>C | NCBI36 |
NG_012166.1:g.5223G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000177694.2:c.12G>C MANE Select | ENSP00000177694.1:p.Val4= | |
ENST00000177694.1:c.12G>C | ENSP00000177694.1:p.Val4= | |
ENST00000581328.1:n.42G>C | ||
NM_013351.1:c.12G>C | NP_037483.1:p.Val4= | |
XM_011524698.1:c.12G>C | XP_011523000.1:p.Val4= | |
NM_013351.2:c.12G>C MANE Select | NP_037483.1:p.Val4= |