HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75764622G>T , CM000676.2:g.75764622G>T | GRCh38 |
NC_000014.8:g.76230965G>T , CM000676.1:g.76230965G>T | GRCh37 |
NC_000014.7:g.75300718G>T | NCBI36 |
NG_016974.1:g.108415G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000298832.14:c.1558G>T MANE Select | ENSP00000298832.9:p.Ala520Ser | |
ENST00000298832.13:c.1558G>T | ENSP00000298832.9:p.Ala520Ser | |
ENST00000554510.5:c.85G>T | ENSP00000451946.1:p.Ala29Ser | |
ENST00000555422.5:n.864G>T | ||
ENST00000556893.5:c.211G>T | ENSP00000452524.1:p.Ala71Ser | |
ENST00000556976.1:n.292G>T | ||
ENST00000557636.5:c.1600G>T | ENSP00000450713.1:p.Ala534Ser | |
NM_015072.4:c.1558G>T | NP_055887.3:p.Ala520Ser | |
NM_015072.5:c.1558G>T MANE Select | NP_055887.3:p.Ala520Ser |