Linked Data
dbSNP Id:
rs1165114591
gnomAD v2:
5-134364510-C-T
gnomAD v3:
5-135028820-C-T
gnomAD v4:
5-135028820-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135028820C>T , CM000667.2:g.135028820C>T | GRCh38 |
| NC_000005.9:g.134364510C>T , CM000667.1:g.134364510C>T | GRCh37 |
| NC_000005.8:g.134392409C>T | NCBI36 |
| NG_012114.1:g.10455G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.904G>A MANE Select | ENSP00000265340.6:p.Gly302Ser | |
| ENST00000265340.11:c.904G>A | ENSP00000265340.6:p.Gly302Ser | |
| ENST00000506438.5:c.904G>A | ENSP00000427542.1:p.Gly302Ser | |
| NM_002653.4:c.904G>A | NP_002644.4:p.Gly302Ser | |
| NM_002653.5:c.904G>A MANE Select | NP_002644.4:p.Gly302Ser |