HGVS | Genome Assembly |
---|---|
NC_000004.12:g.87612362T>G , CM000666.2:g.87612362T>G | GRCh38 |
NC_000004.11:g.88533514T>G , CM000666.1:g.88533514T>G | GRCh37 |
NC_000004.10:g.88752538T>G | NCBI36 |
NG_011595.1:g.8834T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651931.1:c.176T>G MANE Select | ENSP00000498766.1:p.Val59Gly | |
ENST00000282478.7:c.176T>G | ENSP00000282478.7:p.Val59Gly | |
ENST00000399271.5:c.176T>G | ENSP00000382213.1:p.Val59Gly | |
NM_014208.3:c.176T>G MANE Select | NP_055023.2:p.Val59Gly |