HGVS | Genome Assembly |
---|---|
NC_000002.12:g.208124173G>C , CM000664.2:g.208124173G>C | GRCh38 |
NC_000002.11:g.208988897G>C , CM000664.1:g.208988897G>C | GRCh37 |
NC_000002.10:g.208697142G>C | NCBI36 |
NG_008039.1:g.5417C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264376.5:c.191C>G MANE Select | ENSP00000264376.4:p.Ala64Gly | |
ENST00000264376.4:c.191C>G | ENSP00000264376.4:p.Ala64Gly | |
NM_006891.3:c.191C>G | NP_008822.2:p.Ala64Gly | |
NR_038437.1:n.97+4948G>C | ||
NM_006891.4:c.191C>G MANE Select | NP_008822.2:p.Ala64Gly |