Linked Data
gnomAD v4:
1-204190468-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190468C>G , CM000663.2:g.204190468C>G | GRCh38 |
| NC_000001.10:g.204159596C>G , CM000663.1:g.204159596C>G | GRCh37 |
| NC_000001.9:g.202426219C>G | NCBI36 |
| NG_032151.1:g.11024G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*16G>C MANE Select | ENSP00000356162.4:n.*16G>C | |
| ENST00000367194.4:c.*16G>C | ENSP00000356162.4:n.*16G>C | |
| ENST00000625357.1:c.429G>C | ENSP00000485957.1:p.Gly143= | |
| NM_002256.3:c.*16G>C | NP_002247.3:n.*16G>C | |
| XM_011509525.1:c.*16G>C | XP_011507827.1:n.*16G>C | |
| NM_002256.4:c.*16G>C MANE Select | NP_002247.3:n.*16G>C |