HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21600080G>C , CM000669.2:g.21600080G>C | GRCh38 |
NC_000007.13:g.21639698G>C , CM000669.1:g.21639698G>C | GRCh37 |
NC_000007.12:g.21606223G>C | NCBI36 |
NG_012886.2:g.61866G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.2961G>C MANE Select | ENSP00000475939.1:p.Met987Ile | |
ENST00000328843.10:c.2961G>C | ENSP00000330671.7:p.Met987Ile | |
ENST00000409508.7:c.2961G>C | ENSP00000475939.1:p.Met987Ile | |
ENST00000620169.4:c.2961G>C | ENSP00000481693.1:p.Met987Ile | |
NM_001277115.1:c.2961G>C | NP_001264044.1:p.Met987Ile | |
NM_001277115.2:c.2961G>C MANE Select | NP_001264044.1:p.Met987Ile |