HGVS | Genome Assembly |
---|---|
NC_000006.12:g.96057326T= , CM000668.2:g.96057326T= | GRCh38 |
NC_000006.11:g.96505202T= , CM000668.1:g.96505202T= | GRCh37 |
NC_000006.10:g.96611923T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000302103.6:c.-98+41114T= MANE Select | ENSP00000302599.4:n.-98+41114T= | |
ENST00000302103.5:c.-98+41114T= | ENSP00000302599.4:n.-98+41114T= | |
NM_006581.3:c.-98+41114T= | NP_006572.2:n.-98+41114T= | |
XM_011535384.1:c.-98+36353T= | XP_011533686.1:n.-98+36353T= | |
XM_017010190.1:c.-215+41114T= | XP_016865679.1:n.-215+41114T= | |
XR_001744267.2:n.1932A= | ||
NM_006581.4:c.-98+41114T= MANE Select | NP_006572.2:n.-98+41114T= |