HGVS | Genome Assembly |
---|---|
NC_000004.12:g.47406715G>C , CM000666.2:g.47406715G>C | GRCh38 |
NC_000004.11:g.47408732G>C , CM000666.1:g.47408732G>C | GRCh37 |
NC_000004.10:g.47103489G>C | NCBI36 |
NG_051831.1:g.380438G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000295454.8:c.869G>C MANE Select | ENSP00000295454.3:p.Ser290Thr | |
ENST00000295454.7:c.869G>C | ENSP00000295454.3:p.Ser290Thr | |
NM_000812.3:c.869G>C | NP_000803.2:p.Ser290Thr | |
XM_011513678.1:c.848G>C | XP_011511980.1:p.Ser283Thr | |
XM_017007985.1:c.218G>C | XP_016863474.1:p.Ser73Thr | |
XM_024453976.1:c.770G>C | XP_024309744.1:p.Ser257Thr | |
XM_024453977.1:c.770G>C | XP_024309745.1:p.Ser257Thr | |
XM_024453978.1:c.770G>C | XP_024309746.1:p.Ser257Thr | |
NM_000812.4:c.869G>C MANE Select | NP_000803.2:p.Ser290Thr |