HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135798100A= , CM000664.2:g.135798100A= | GRCh38 |
NC_000002.11:g.136555670A= , CM000664.1:g.136555670A= | GRCh37 |
NC_000002.10:g.136272140A= | NCBI36 |
NG_008104.2:g.62070T= , LRG_338:g.62070T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264162.7:c.4905T= MANE Select | ENSP00000264162.2:p.Asn1635= | |
ENST00000264162.6:c.4905T= | ENSP00000264162.2:p.Asn1635= | |
ENST00000452974.1:c.2998T= | ENSP00000391231.1:p.Trp1000= | |
NM_002299.2:c.4905T= , LRG_338t1:c.4905T= | NP_002290.2:p.Asn1635= | |
NM_002299.3:c.4905T= | NP_002290.2:p.Asn1635= | |
XM_017004088.2:c.4905T= | XP_016859577.1:p.Asn1635= | |
NM_002299.4:c.4905T= MANE Select | NP_002290.2:p.Asn1635= |