HGVS | Genome Assembly |
---|---|
NC_000020.11:g.57562940G= , CM000682.2:g.57562940G= | GRCh38 |
NC_000020.10:g.56137996G= , CM000682.1:g.56137996G= | GRCh37 |
NC_000020.9:g.55571402G= | NCBI36 |
NG_008205.1:g.6860G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319441.6:c.610+41G= MANE Select | ENSP00000319814.4:n.610+41G= | |
ENST00000319441.5:c.610+41G= | ENSP00000319814.4:n.610+41G= | |
ENST00000467047.1:n.1861G= | ||
ENST00000470051.1:n.107G= | ||
ENST00000498194.1:n.552+41G= | ||
NM_002591.3:c.610+41G= | NP_002582.3:n.610+41G= | |
XM_011528839.1:c.214+41G= | XP_011527141.1:n.214+41G= | |
XM_024451888.1:c.214+41G= | XP_024307656.1:n.214+41G= | |
NM_002591.4:c.610+41G= MANE Select | NP_002582.3:n.610+41G= |