Linked Data
gnomAD v4:
5-135028873-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135028873C>G , CM000667.2:g.135028873C>G | GRCh38 |
| NC_000005.9:g.134364563C>G , CM000667.1:g.134364563C>G | GRCh37 |
| NC_000005.8:g.134392462C>G | NCBI36 |
| NG_012114.1:g.10402G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.851G>C MANE Select | ENSP00000265340.6:p.Ser284Thr | |
| ENST00000265340.11:c.851G>C | ENSP00000265340.6:p.Ser284Thr | |
| ENST00000506438.5:c.851G>C | ENSP00000427542.1:p.Ser284Thr | |
| NM_002653.4:c.851G>C | NP_002644.4:p.Ser284Thr | |
| NM_002653.5:c.851G>C MANE Select | NP_002644.4:p.Ser284Thr |