Linked Data
dbSNP Id:
rs1245580278
gnomAD v2:
5-134364450-G-A
gnomAD v3:
5-135028760-G-A
gnomAD v4:
5-135028760-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135028760G>A , CM000667.2:g.135028760G>A | GRCh38 |
| NC_000005.9:g.134364450G>A , CM000667.1:g.134364450G>A | GRCh37 |
| NC_000005.8:g.134392349G>A | NCBI36 |
| NG_012114.1:g.10515C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.*19C>T MANE Select | ENSP00000265340.6:n.*19C>T | |
| ENST00000265340.11:c.*19C>T | ENSP00000265340.6:n.*19C>T | |
| ENST00000506438.5:c.*19C>T | ENSP00000427542.1:n.*19C>T | |
| NM_002653.4:c.*19C>T | NP_002644.4:n.*19C>T | |
| NM_002653.5:c.*19C>T MANE Select | NP_002644.4:n.*19C>T |