HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135798038T= , CM000664.2:g.135798038T= | GRCh38 |
NC_000002.11:g.136555608T= , CM000664.1:g.136555608T= | GRCh37 |
NC_000002.10:g.136272078T= | NCBI36 |
NG_008104.2:g.62132A= , LRG_338:g.62132A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264162.7:c.4967A= MANE Select | ENSP00000264162.2:p.Asn1656= | |
ENST00000264162.6:c.4967A= | ENSP00000264162.2:p.Asn1656= | |
ENST00000452974.1:c.3060A= | ENSP00000391231.1:n.3060A= | |
NM_002299.2:c.4967A= , LRG_338t1:c.4967A= | NP_002290.2:p.Asn1656= | |
NM_002299.3:c.4967A= | NP_002290.2:p.Asn1656= | |
XM_017004088.2:c.4967A= | XP_016859577.1:p.Asn1656= | |
NM_002299.4:c.4967A= MANE Select | NP_002290.2:p.Asn1656= |