HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48492389A>G , CM000677.2:g.48492389A>G | GRCh38 |
NC_000015.9:g.48784586A>G , CM000677.1:g.48784586A>G | GRCh37 |
NC_000015.8:g.46571878A>G | NCBI36 |
NG_008805.2:g.158400T>C , LRG_778:g.158400T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.2854+72T>C | ENSP00000453958.2:n.2854+72T>C | |
ENST00000674301.2:c.2854+72T>C | ENSP00000501333.2:n.2854+72T>C | |
ENST00000684448.1:n.1528+72T>C | ||
ENST00000316623.10:c.2854+72T>C MANE Select | ENSP00000325527.5:n.2854+72T>C | |
ENST00000316623.9:c.2854+72T>C | ENSP00000325527.5:n.2854+72T>C | |
ENST00000537463.6:c.637-17739T>C | ENSP00000440294.2:n.637-17739T>C | |
NM_000138.4:c.2854+72T>C , LRG_778t1:c.2854+72T>C | NP_000129.3:n.2854+72T>C | |
NM_000138.5:c.2854+72T>C MANE Select | NP_000129.3:n.2854+72T>C |