HGVS | Genome Assembly |
---|---|
NC_000010.11:g.61992321T= , CM000672.2:g.61992321T= | GRCh38 |
NC_000010.10:g.63752080T= , CM000672.1:g.63752080T= | GRCh37 |
NC_000010.9:g.63422086T= | NCBI36 |
NG_030027.1:g.96068T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000279873.12:c.503-7770T= MANE Select | ENSP00000279873.7:n.503-7770T= | |
ENST00000644638.1:c.503-7770T= | ENSP00000494412.1:n.503-7770T= | |
ENST00000681100.1:c.503-7770T= | ENSP00000506119.1:n.503-7770T= | |
ENST00000279873.11:c.503-7770T= | ENSP00000279873.7:n.503-7770T= | |
NM_032199.2:c.503-7770T= | NP_115575.1:n.503-7770T= | |
XM_011540262.1:c.502+51913T= | XP_011538564.1:n.502+51913T= | |
XM_024448230.1:c.-65-7770T= | XP_024303998.1:n.-65-7770T= | |
NM_032199.3:c.503-7770T= MANE Select | NP_115575.1:n.503-7770T= |