HGVS | Genome Assembly |
---|---|
NC_000002.12:g.215064025A= , CM000664.2:g.215064025A= | GRCh38 |
NC_000002.11:g.215928748A= , CM000664.1:g.215928748A= | GRCh37 |
NC_000002.10:g.215636993A= | NCBI36 |
NG_007074.1:g.79404T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000272895.12:c.317+41T= MANE Select | ENSP00000272895.7:n.317+41T= | |
ENST00000272895.11:c.317+41T= | ENSP00000272895.7:n.317+41T= | |
NM_173076.2:c.317+41T= | NP_775099.2:n.317+41T= | |
NR_103740.1:n.537+41T= | ||
XM_011510951.1:c.317+41T= | XP_011509253.1:n.317+41T= | |
XM_011510952.1:c.317+41T= | XP_011509254.1:n.317+41T= | |
XM_011510951.2:c.317+41T= | XP_011509253.1:n.317+41T= | |
NM_173076.3:c.317+41T= MANE Select | NP_775099.2:n.317+41T= | |
NR_103740.2:n.735+41T= |