Linked Data
dbSNP Id:
rs1766182313
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140333378A>G , CM000667.2:g.140333378A>G | GRCh38 |
| NC_000005.9:g.139712963A>G , CM000667.1:g.139712963A>G | GRCh37 |
| NC_000005.8:g.139693147A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230990.7:c.*921T>C MANE Select | ENSP00000230990.6:n.*921T>C | |
| ENST00000230990.6:c.*921T>C | ENSP00000230990.6:n.*921T>C | |
| NM_001945.2:c.*921T>C | NP_001936.1:n.*921T>C | |
| NM_001945.3:c.*921T>C MANE Select | NP_001936.1:n.*921T>C |