HGVS | Genome Assembly |
---|---|
NC_000013.11:g.113119017C= , CM000675.2:g.113119017C= | GRCh38 |
NC_000013.10:g.113773331C= , CM000675.1:g.113773331C= | GRCh37 |
NC_000013.9:g.112821332C= | NCBI36 |
NG_009258.1:g.1219C= , LRG_548:g.1219C= | |
NG_009262.1:g.18227C= , LRG_554:g.18227C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000346342.8:c.*9C= MANE Select | ENSP00000329546.4:n.*9C= | |
ENST00000346342.7:c.*9C= | ENSP00000329546.3:n.*9C= | |
ENST00000375581.3:c.*9C= | ENSP00000364731.3:n.*9C= | |
ENST00000541084.5:c.*9C= | ENSP00000442051.2:n.*9C= | |
NM_000131.4:c.*9C= , LRG_554t1:c.*9C= | NP_000122.1:n.*9C= | |
NM_001267554.1:c.*9C= | NP_001254483.1:n.*9C= | |
NM_019616.3:c.*9C= , LRG_554t2:c.*9C= | NP_062562.1:n.*9C= | |
NR_051961.1:n.1431C= | ||
XM_006719963.2:c.*9C= | XP_006720026.1:n.*9C= | |
XM_011537474.1:c.*9C= | XP_011535776.1:n.*9C= | |
XM_011537475.1:c.*9C= | XP_011535777.1:n.*9C= | |
XM_011537476.1:c.*9C= | XP_011535778.1:n.*9C= | |
XM_011537477.1:c.*9C= | XP_011535779.1:n.*9C= | |
XM_006719963.3:c.*9C= | XP_006720026.2:n.*9C= | |
XM_011537474.2:c.*9C= | XP_011535776.2:n.*9C= | |
XM_011537475.2:c.*9C= | XP_011535777.2:n.*9C= | |
XM_011537476.2:c.*9C= | XP_011535778.1:n.*9C= | |
NM_019616.4:c.*9C= MANE Select | NP_062562.1:n.*9C= | |
NR_051961.2:n.1428C= | ||
NM_001267554.2:c.*9C= | NP_001254483.1:n.*9C= |