HGVS | Genome Assembly |
---|---|
NC_000003.12:g.122341447A>C , CM000665.2:g.122341447A>C | GRCh38 |
NC_000003.11:g.122060294A>C , CM000665.1:g.122060294A>C | GRCh37 |
NC_000003.10:g.123542984A>C | NCBI36 |
NG_027995.1:g.21284A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264474.4:c.177A>C MANE Select | ENSP00000264474.3:p.Ala59= | |
ENST00000264474.3:c.177A>C | ENSP00000264474.3:p.Ala59= | |
NM_005213.3:c.177A>C | NP_005204.1:p.Ala59= | |
NM_005213.4:c.177A>C MANE Select | NP_005204.1:p.Ala59= |