HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48537540A>G , CM000677.2:g.48537540A>G | GRCh38 |
NC_000015.9:g.48829737A>G , CM000677.1:g.48829737A>G | GRCh37 |
NC_000015.8:g.46617029A>G | NCBI36 |
NG_008805.2:g.113249T>C , LRG_778:g.113249T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000559133.6:c.736+71T>C | ENSP00000453958.2:n.736+71T>C | |
ENST00000674301.2:c.736+71T>C | ENSP00000501333.2:n.736+71T>C | |
ENST00000316623.10:c.736+71T>C MANE Select | ENSP00000325527.5:n.736+71T>C | |
ENST00000316623.9:c.736+71T>C | ENSP00000325527.5:n.736+71T>C | |
ENST00000537463.6:c.636+171T>C | ENSP00000440294.2:n.636+171T>C | |
NM_000138.4:c.736+71T>C , LRG_778t1:c.736+71T>C | NP_000129.3:n.736+71T>C | |
NM_000138.5:c.736+71T>C MANE Select | NP_000129.3:n.736+71T>C |