HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32104716T>C , CM000684.2:g.32104716T>C | GRCh38 |
NC_000022.10:g.32500703T>C , CM000684.1:g.32500703T>C | GRCh37 |
NC_000022.9:g.30830703T>C | NCBI36 |
NG_017045.1:g.66685T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266088.9:c.1666-70T>C MANE Select | ENSP00000266088.4:n.1666-70T>C | |
ENST00000266088.8:c.1666-70T>C | ENSP00000266088.4:n.1666-70T>C | |
ENST00000543737.2:c.1285-70T>C | ENSP00000444898.1:n.1285-70T>C | |
NM_000343.3:c.1666-70T>C | NP_000334.1:n.1666-70T>C | |
NM_001256314.1:c.1285-70T>C | NP_001243243.1:n.1285-70T>C | |
XR_938173.1:n.591+2122A>G | ||
XR_938174.1:n.486+15139A>G | ||
NM_000343.4:c.1666-70T>C MANE Select | NP_000334.1:n.1666-70T>C | |
NM_001256314.2:c.1285-70T>C | NP_001243243.1:n.1285-70T>C |