HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110602029G>T , CM000672.2:g.110602029G>T | GRCh38 |
NC_000010.10:g.112361787G>T , CM000672.1:g.112361787G>T | GRCh37 |
NC_000010.9:g.112351777G>T | NCBI36 |
NG_012217.1:g.39339G>T , LRG_774:g.39339G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.5189G>T | ||
ENST00000685743.1:n.2664G>T | ||
ENST00000686057.1:n.1307G>T | ||
ENST00000689321.1:n.1919G>T | ||
ENST00000689986.1:n.745G>T | ||
ENST00000361804.5:c.2956G>T MANE Select | ENSP00000354720.5:p.Ala986Ser | |
ENST00000361804.4:c.2956G>T | ENSP00000354720.4:p.Ala986Ser | |
NM_005445.3:c.2956G>T , LRG_774t1:c.2956G>T | NP_005436.1:p.Ala986Ser | |
NM_005445.4:c.2956G>T MANE Select | NP_005436.1:p.Ala986Ser |