HGVS | Genome Assembly |
---|---|
NC_000008.11:g.64624502G>A , CM000670.2:g.64624502G>A | GRCh38 |
NC_000008.10:g.65537059G>A , CM000670.1:g.65537059G>A | GRCh37 |
NC_000008.9:g.65699613G>A | NCBI36 |
NG_008338.1:g.179290C>T | |
NG_008338.2:g.179290C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000310193.4:c.160C>T MANE Select | ENSP00000310721.3:p.Pro54Ser | |
ENST00000310193.3:c.160C>T | ENSP00000310721.3:p.Pro54Ser | |
NM_004820.3:c.160C>T | NP_004811.1:p.Pro54Ser | |
NM_001324112.1:c.160C>T | NP_001311041.1:p.Pro54Ser | |
NM_004820.4:c.160C>T | NP_004811.1:p.Pro54Ser | |
XM_017014002.1:c.226C>T | XP_016869491.1:p.Pro76Ser | |
NM_004820.5:c.160C>T MANE Select | NP_004811.1:p.Pro54Ser | |
NM_001324112.2:c.160C>T | NP_001311041.1:p.Pro54Ser |