HGVS | Genome Assembly |
---|---|
NC_000012.12:g.111803870A>C , CM000674.2:g.111803870A>C | GRCh38 |
NC_000012.11:g.112241674A>C , CM000674.1:g.112241674A>C | GRCh37 |
NC_000012.10:g.110726057A>C | NCBI36 |
NG_012250.1:g.42329A>C | |
NG_012250.2:g.41984A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261733.7:c.1418A>C MANE Select | ENSP00000261733.2:p.Tyr473Ser | |
ENST00000261733.6:c.1418A>C | ENSP00000261733.2:p.Tyr473Ser | |
ENST00000416293.7:c.1277A>C | ENSP00000403349.3:p.Tyr426Ser | |
ENST00000548536.1:c.*1294A>C | ENSP00000448179.1:n.*1294A>C | |
ENST00000549106.1:c.349A>C | ||
NM_000690.3:c.1418A>C | NP_000681.2:p.Tyr473Ser | |
NM_001204889.1:c.1277A>C | NP_001191818.1:p.Tyr426Ser | |
NM_000690.4:c.1418A>C MANE Select | NP_000681.2:p.Tyr473Ser | |
NM_001204889.2:c.1277A>C | NP_001191818.1:p.Tyr426Ser |