HGVS | Genome Assembly |
---|---|
NC_000016.10:g.46698064G>A , CM000678.2:g.46698064G>A | GRCh38 |
NC_000016.9:g.46731976G>A , CM000678.1:g.46731976G>A | GRCh37 |
NC_000016.8:g.45289477G>A | NCBI36 |
NG_028241.1:g.13419G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000219097.7:c.*479G>A MANE Select | ENSP00000219097.2:n.*479G>A | |
ENST00000219097.6:c.*479G>A | ENSP00000219097.2:n.*479G>A | |
ENST00000566860.1:c.*479G>A | ENSP00000456981.1:n.*479G>A | |
ENST00000567000.2:n.1242G>A | ||
NM_014321.3:c.*479G>A | NP_055136.1:n.*479G>A | |
NR_037620.1:n.1357G>A | ||
NM_014321.4:c.*479G>A MANE Select | NP_055136.1:n.*479G>A | |
NR_037620.2:n.1344G>A |