HGVS | Genome Assembly |
---|---|
NC_000006.12:g.96057388G= , CM000668.2:g.96057388G= | GRCh38 |
NC_000006.11:g.96505264G= , CM000668.1:g.96505264G= | GRCh37 |
NC_000006.10:g.96611985G= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000302103.6:c.-98+41176G= MANE Select | ENSP00000302599.4:n.-98+41176G= | |
ENST00000302103.5:c.-98+41176G= | ENSP00000302599.4:n.-98+41176G= | |
NM_006581.3:c.-98+41176G= | NP_006572.2:n.-98+41176G= | |
XM_011535384.1:c.-98+36415G= | XP_011533686.1:n.-98+36415G= | |
XM_017010190.1:c.-215+41176G= | XP_016865679.1:n.-215+41176G= | |
XR_001744267.2:n.1870C= | ||
NM_006581.4:c.-98+41176G= MANE Select | NP_006572.2:n.-98+41176G= |