HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240873211C= , CM000664.2:g.240873211C= | GRCh38 |
NC_000002.11:g.241812628C= , CM000664.1:g.241812628C= | GRCh37 |
NC_000002.10:g.241461301C= | NCBI36 |
NG_008005.1:g.9467C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.595+162C= MANE Select | ENSP00000302620.3:n.595+162C= | |
ENST00000307503.3:c.595+162C= | ENSP00000302620.3:n.595+162C= | |
ENST00000472436.1:n.777C= | ||
ENST00000476698.1:n.332+162C= | ||
NM_000030.2:c.595+162C= | NP_000021.1:n.595+162C= | |
NM_000030.3:c.595+162C= MANE Select | NP_000021.1:n.595+162C= |