HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6023702G>C , CM000674.2:g.6023702G>C | GRCh38 |
NC_000012.11:g.6132868G>C , CM000674.1:g.6132868G>C | GRCh37 |
NC_000012.10:g.6003129G>C | NCBI36 |
NG_009072.1:g.105969C>G | |
NG_009072.2:g.105969C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.3308C>G MANE Select | ENSP00000261405.5:p.Thr1103Ser | |
ENST00000261405.9:c.3308C>G | ENSP00000261405.5:p.Thr1103Ser | |
ENST00000538635.5:n.421-29768C>G | ||
NM_000552.3:c.3308C>G | NP_000543.2:p.Thr1103Ser | |
NM_000552.4:c.3308C>G | NP_000543.2:p.Thr1103Ser | |
NM_000552.5:c.3308C>G MANE Select | NP_000543.3:p.Thr1103Ser |