HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117069C>G , CM000669.2:g.19117069C>G | GRCh38 |
NC_000007.13:g.19156692C>G , CM000669.1:g.19156692C>G | GRCh37 |
NC_000007.12:g.19123217C>G | NCBI36 |
NG_008114.1:g.5604G>C | |
NG_008114.2:g.5604G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.253G>C MANE Select | ENSP00000242261.5:p.Gly85Arg | |
ENST00000242261.5:c.253G>C | ENSP00000242261.5:p.Gly85Arg | |
ENST00000354571.5:c.50G>C | ||
NM_000474.3:c.253G>C | NP_000465.1:p.Gly85Arg | |
XM_011515496.1:c.253G>C | XP_011513798.1:p.Gly85Arg | |
NR_149001.1:n.604G>C | ||
NM_000474.4:c.253G>C MANE Select | NP_000465.1:p.Gly85Arg | |
NR_149001.2:n.568G>C |