HGVS | Genome Assembly |
---|---|
NC_000004.12:g.40354345A>T , CM000666.2:g.40354345A>T | GRCh38 |
NC_000004.11:g.40356362A>T , CM000666.1:g.40356362A>T | GRCh37 |
NC_000004.10:g.40051119A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000310169.3:c.1265A>T MANE Select | ENSP00000312663.2:p.Lys422Ile | |
ENST00000310169.2:c.1265A>T | ENSP00000312663.2:p.Lys422Ile | |
NM_017581.3:c.1265A>T | NP_060051.2:p.Lys422Ile | |
NM_017581.4:c.1265A>T MANE Select | NP_060051.2:p.Lys422Ile |