Linked Data
dbSNP Id:
rs940725202
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714253G>A , CM000681.2:g.6714253G>A | GRCh38 |
| NC_000019.9:g.6714264G>A , CM000681.1:g.6714264G>A | GRCh37 |
| NC_000019.8:g.6665264G>A | NCBI36 |
| NG_009557.1:g.11399C>T , LRG_27:g.11399C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.477-5C>T | ENSP00000512083.1:n.477-5C>T | |
| ENST00000245907.11:c.600-5C>T MANE Select | ENSP00000245907.4:n.600-5C>T | |
| ENST00000245907.10:c.600-5C>T | ENSP00000245907.4:n.600-5C>T | |
| ENST00000595577.1:n.99C>T | ||
| NM_000064.3:c.600-5C>T | NP_000055.2:n.600-5C>T | |
| NM_000064.4:c.600-5C>T MANE Select | NP_000055.2:n.600-5C>T |