Linked Data
dbSNP Id:
rs1290064187
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.157421729T>A , CM000664.2:g.157421729T>A | GRCh38 |
| NC_000002.11:g.158278241T>A , CM000664.1:g.158278241T>A | GRCh37 |
| NC_000002.10:g.157986487T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264192.8:c.547-3140A>T MANE Select | ENSP00000264192.3:n.547-3140A>T | |
| ENST00000264192.7:c.547-3140A>T | ENSP00000264192.3:n.547-3140A>T | |
| ENST00000418920.5:c.229-3140A>T | ENSP00000394308.1:n.229-3140A>T | |
| ENST00000457793.6:c.*442-3140A>T | ENSP00000407205.2:n.*442-3140A>T | |
| NM_004288.4:c.547-3140A>T | NP_004279.3:n.547-3140A>T | |
| XM_017005386.2:c.229-3140A>T | XP_016860875.1:n.229-3140A>T | |
| NM_004288.5:c.547-3140A>T MANE Select | NP_004279.3:n.547-3140A>T |