Linked Data
gnomAD v4:
5-135028828-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135028828C>T , CM000667.2:g.135028828C>T | GRCh38 |
| NC_000005.9:g.134364518C>T , CM000667.1:g.134364518C>T | GRCh37 |
| NC_000005.8:g.134392417C>T | NCBI36 |
| NG_012114.1:g.10447G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.896G>A MANE Select | ENSP00000265340.6:p.Gly299Asp | |
| ENST00000265340.11:c.896G>A | ENSP00000265340.6:p.Gly299Asp | |
| ENST00000506438.5:c.896G>A | ENSP00000427542.1:p.Gly299Asp | |
| NM_002653.4:c.896G>A | NP_002644.4:p.Gly299Asp | |
| NM_002653.5:c.896G>A MANE Select | NP_002644.4:p.Gly299Asp |