HGVS | Genome Assembly |
---|---|
NC_000005.10:g.14716565T>C , CM000667.2:g.14716565T>C | GRCh38 |
NC_000005.9:g.14716674T>C , CM000667.1:g.14716674T>C | GRCh37 |
NC_000005.8:g.14769674T>C | NCBI36 |
NG_008273.1:g.160214A>G | |
NG_008273.2:g.160221A>G | |
NG_051625.1:g.60772T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000284268.8:c.1141+141A>G MANE Select | ENSP00000284268.6:n.1141+141A>G | |
ENST00000284268.6:c.1141+141A>G | ENSP00000284268.6:n.1141+141A>G | |
ENST00000502585.1:n.383+141A>G | ||
NM_054027.4:c.1141+141A>G | NP_473368.1:n.1141+141A>G | |
NM_054027.5:c.1141+141A>G | NP_473368.1:n.1141+141A>G | |
XM_017009644.2:c.1057+141A>G | XP_016865133.1:n.1057+141A>G | |
NM_054027.6:c.1141+141A>G MANE Select | NP_473368.1:n.1141+141A>G |