HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49459498G>T , CM000668.2:g.49459498G>T | GRCh38 |
NC_000006.11:g.49427211G>T , CM000668.1:g.49427211G>T | GRCh37 |
NC_000006.10:g.49535170G>T | NCBI36 |
NG_007100.1:g.8642C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.-32C>A MANE Select | ENSP00000274813.3:n.-32C>A | |
ENST00000274813.3:c.-32C>A | ENSP00000274813.3:n.-32C>A | |
NM_000255.3:c.-32C>A | NP_000246.2:n.-32C>A | |
XM_005249143.2:c.-32C>A | XP_005249200.1:n.-32C>A | |
XM_005249143.3:c.-32C>A | XP_005249200.1:n.-32C>A | |
NM_000255.4:c.-32C>A MANE Select | NP_000246.2:n.-32C>A |