HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65240057A>G , CM000674.2:g.65240057A>G | GRCh38 |
NC_000012.11:g.65633837A>G , CM000674.1:g.65633837A>G | GRCh37 |
NC_000012.10:g.63920104A>G | NCBI36 |
NG_016210.1:g.75487A>G | |
NG_016210.2:g.75487A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.2023+27A>G MANE Select | ENSP00000308369.2:n.2023+27A>G | |
ENST00000308330.2:c.2023+27A>G | ENSP00000308369.2:n.2023+27A>G | |
NM_001167614.1:c.2020+27A>G | NP_001161086.1:n.2020+27A>G | |
NM_014319.4:c.2023+27A>G | NP_055134.2:n.2023+27A>G | |
NM_014319.5:c.2023+27A>G MANE Select | NP_055134.2:n.2023+27A>G | |
NM_001167614.2:c.2020+27A>G | NP_001161086.1:n.2020+27A>G |