Linked Data
dbSNP Id:
rs186322246
gnomAD v2:
16-31102291-C-A
gnomAD v3:
16-31090970-C-A
gnomAD v4:
16-31090970-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.31090970C>A , CM000678.2:g.31090970C>A | GRCh38 |
| NC_000016.9:g.31102291C>A , CM000678.1:g.31102291C>A | GRCh37 |
| NC_000016.8:g.31009792C>A | NCBI36 |
| NG_011564.1:g.8986G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394975.3:c.*164G>T MANE Select | ENSP00000378426.2:n.*164G>T | |
| ENST00000300851.10:c.*267G>T | ENSP00000300851.6:n.*267G>T | |
| ENST00000319788.11:c.*267G>T | ENSP00000326135.7:n.*267G>T | |
| ENST00000354895.4:c.*267G>T | ENSP00000346969.4:n.*267G>T | |
| ENST00000394975.2:c.*164G>T | ENSP00000378426.2:n.*164G>T | |
| ENST00000420057.2:c.618G>T | ||
| ENST00000529564.1:c.283+2342G>T | ENSP00000431371.1:n.283+2342G>T | |
| ENST00000532364.1:c.173+3587G>T | ENSP00000460316.1:n.173+3587G>T | |
| ENST00000533518.5:c.407+122G>T | ||
| NM_001311311.1:c.*164G>T | NP_001298240.1:n.*164G>T | |
| NM_024006.4:c.*164G>T | NP_076869.1:n.*164G>T | |
| NM_024006.5:c.*164G>T | NP_076869.1:n.*164G>T | |
| NM_206824.1:c.*267G>T | NP_996560.1:n.*267G>T | |
| NM_206824.2:c.*267G>T | NP_996560.1:n.*267G>T | |
| XM_011545944.1:c.*164G>T | XP_011544246.1:n.*164G>T | |
| XM_011545945.1:c.*267G>T | XP_011544247.1:n.*267G>T | |
| XR_950848.1:n.1444G>T | ||
| NM_024006.6:c.*164G>T MANE Select | NP_076869.1:n.*164G>T | |
| NM_001311311.2:c.*164G>T | NP_001298240.1:n.*164G>T | |
| NM_206824.3:c.*267G>T | NP_996560.1:n.*267G>T |