HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48965765C>G , CM000681.2:g.48965765C>G | GRCh38 |
NC_000019.9:g.49469022C>G , CM000681.1:g.49469022C>G | GRCh37 |
NC_000019.8:g.54160834C>G | NCBI36 |
NG_008152.1:g.5457C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000331825.11:c.103-5C>G MANE Select | ENSP00000366525.2:n.103-5C>G | |
ENST00000331825.10:c.103-5C>G | ENSP00000366525.2:n.103-5C>G | |
ENST00000622577.2:c.103-5C>G | ENSP00000484043.1:n.103-5C>G | |
NM_000146.3:c.103-5C>G | NP_000137.2:n.103-5C>G | |
XM_024451447.1:c.613-5C>G | XP_024307215.1:n.613-5C>G | |
NM_000146.4:c.103-5C>G MANE Select | NP_000137.2:n.103-5C>G |