HGVS | Genome Assembly |
---|---|
NC_000004.12:g.40354461T>G , CM000666.2:g.40354461T>G | GRCh38 |
NC_000004.11:g.40356478T>G , CM000666.1:g.40356478T>G | GRCh37 |
NC_000004.10:g.40051235T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000310169.3:c.1381T>G MANE Select | ENSP00000312663.2:p.Trp461Gly | |
ENST00000310169.2:c.1381T>G | ENSP00000312663.2:p.Trp461Gly | |
NM_017581.3:c.1381T>G | NP_060051.2:p.Trp461Gly | |
NM_017581.4:c.1381T>G MANE Select | NP_060051.2:p.Trp461Gly |