HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110578663G>C , CM000672.2:g.110578663G>C | GRCh38 |
NC_000010.10:g.112338421G>C , CM000672.1:g.112338421G>C | GRCh37 |
NC_000010.9:g.112328411G>C | NCBI36 |
NG_012217.1:g.15973G>C , LRG_774:g.15973G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.519G>C | ||
ENST00000687823.1:n.300G>C | ||
ENST00000689932.1:n.2449G>C | ||
ENST00000691297.1:n.519G>C | ||
ENST00000691527.1:n.1189G>C | ||
ENST00000692792.1:n.505G>C | ||
ENST00000361804.5:c.386G>C MANE Select | ENSP00000354720.5:p.Gly129Ala | |
ENST00000361804.4:c.386G>C | ENSP00000354720.4:p.Gly129Ala | |
ENST00000462899.1:n.532G>C | ||
NM_005445.3:c.386G>C , LRG_774t1:c.386G>C | NP_005436.1:p.Gly129Ala | |
NM_005445.4:c.386G>C MANE Select | NP_005436.1:p.Gly129Ala |