HGVS | Genome Assembly |
---|---|
NC_000004.12:g.57047012C= , CM000666.2:g.57047012C= | GRCh38 |
NC_000004.11:g.57913178C= , CM000666.1:g.57913178C= | GRCh37 |
NC_000004.10:g.57607935C= | NCBI36 |
NG_031877.1:g.68374G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000295666.6:c.476-6079G= MANE Select | ENSP00000295666.4:n.476-6079G= | |
ENST00000512512.3:n.116-6079G= | ||
ENST00000514062.2:c.476-6079G= | ENSP00000486293.1:n.476-6079G= | |
NM_001253835.1:c.476-6079G= | NP_001240764.1:n.476-6079G= | |
NM_001553.2:c.476-6079G= | NP_001544.1:n.476-6079G= | |
NM_001553.3:c.476-6079G= MANE Select | NP_001544.1:n.476-6079G= | |
NM_001253835.2:c.476-6079G= | NP_001240764.1:n.476-6079G= |