HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135798092T>A , CM000664.2:g.135798092T>A | GRCh38 |
NC_000002.11:g.136555662T>A , CM000664.1:g.136555662T>A | GRCh37 |
NC_000002.10:g.136272132T>A | NCBI36 |
NG_008104.2:g.62078A>T , LRG_338:g.62078A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264162.7:c.4913A>T MANE Select | ENSP00000264162.2:p.Tyr1638Phe | |
ENST00000264162.6:c.4913A>T | ENSP00000264162.2:p.Tyr1638Phe | |
ENST00000452974.1:c.3006A>T | ENSP00000391231.1:p.Leu1002Phe | |
NM_002299.2:c.4913A>T , LRG_338t1:c.4913A>T | NP_002290.2:p.Tyr1638Phe | |
NM_002299.3:c.4913A>T | NP_002290.2:p.Tyr1638Phe | |
XM_017004088.2:c.4913A>T | XP_016859577.1:p.Tyr1638Phe | |
NM_002299.4:c.4913A>T MANE Select | NP_002290.2:p.Tyr1638Phe |